282/2012 Sb.
DECREE
of 21 June 1999. August 2012,
amending the Decree of the Ministry of industry and trade no. 328/2000
Coll. on the method of making certain types of prepacked goods whose
the quantity is expressed in units of weight or volume, as amended by
Decree No. 404/2008 Coll.
The Ministry of industry and trade shall be determined according to section 27 of Act No. 505/1990
Coll. on metrology, as amended by Act No. 119/2000 Coll. and Act No. 137/2002
Coll., to implement section 9a, paragraph 2. 2 to 4:
Article. (I)
Decree 328/2000 Coll. on the method of making certain types of cash
packaged goods, the quantity of which is expressed in units of weight or
volume, as amended by Decree No. 404/2008 Coll., is amended as follows:
1. § 1, including footnote No 1 is added:
"§ 1
This Decree incorporates the relevant provisions of the European Union ^ 1) and
provides:
and construction) requirements for prepackages (hereinafter referred to as "finished
package "), which the importer or packer intends to refer to the symbol" e "
that contains the product intended for sale in constant unit
nominal quantities
1. is equal to the value specified in advance by the Packer,
2. is expressed in units of weight or volume and
3. is not less than 5 g or 5 ml and not more than 10 kg or 10 l, and
(b)) the permissible nominal volumes of certain liquid products that are
contained in the prepackage, regardless of whether the prepackage is
or is not a known symbol "e".
1) Council Directive 76/211/EEC of 20 December. January 1976 on the approximation of
laws of the Member States relating to the making-up of some of the products in
prepackaged products by weight or volume.
European Parliament and Council Directive 2007/45/EC of 5 July 2004. September 2007,
laying down rules on nominal quantities for products in the finished
packaging, repealing Council Directives 75/106/EEC and 80/232/EEC and amending Directive
Council 76/211/EEC. '.
2. section 2 is repealed.
3. in section 3, paragraphs 1 and 2, including footnote 2 shall be added:
"(1) the symbol" e ", whose graphic design provides for a specific legal
prescription ^ 2), you can only mark a prepackage which meets the requirements
Annex No. 1 to the present Decree.
(2) in addition to the obligations referred to in paragraph 1 of the finished packaging marked with the symbol
"e",
and that includes liquid products), must be accompanied by an indication of the
the nominal volume of the product contained in a prepackage, or
(b)) that contains non-liquid products must bear an indication of the
the nominal weight of the product, which is contained in the prepackage.
Exceptions are the cases where it is otherwise provided for commercial usage.
2) Decree No. 262/2000 Coll., which ensures consistency and accuracy
measuring instruments and measurements, as amended. ".
4. In article 3, paragraph 3. 4, after the words "prepackages" words "marked
the symbol "e" ".
5. In § 3a paragraph 2. 1 the words "into circulation" shall be replaced by "on the market" and the word
"quantities" shall be replaced by the word "volume".
6. the annex No. 1 to 3, including the footnotes # 3-14:
' Annex 1 to the Decree No 328/2000 Sb.
REQUIREMENTS FOR PREPACKAGES
1.
The REQUIREMENTS of the
Prepackages marked with the symbol "e" subject to this notice shall be
made so as to complete the packaging levy meets the following requirements:
1.1 the average actual contents of the prepackages in the batch shall be not less
than the nominal quantity of the prepackage;
1.2 in order to meet the requirements of the tests specified in annex No. 2,
must be the proportion of prepackages having a larger negative
deviation of content than the tolerable negative error content referred to in paragraph
2.4, a small part of enough batches of prepackages;
1.3. the symbol "e", whose specification is indicated in section 3.3, shall not be
a dose of the latter no prepackage, that shows a negative deviation
content greater than twice the tolerable negative error
obsahuuvedené in the table in point 2.4.
2.
DEFINITIONS AND BASIC PROVISIONS
2.1 the nominal quantity (nominal weight or nominal volume) of the contents of the
a prepackage is the quantity of the product, expressed in units of
the weight or volume that is indicated on the prepackage, i.e.. such
quantity of the product to which it is assumed that is prepackaged
contained.
2.2. the actual contents of the prepackage are the quantity (weight or volume)
product which it in fact contains. When all of the
control operations focused on the quantity of the product as referred to in
units of volume must be the value of the actual contents of measured at a temperature of
or corrected to a temperature of 20 ° c, no matter at what temperature to
custom packaging or checking is carried out. It does not apply to frozen or
at very low temperatures, frozen products, whose amount is shown in the
units of volume.
2.3. the Negative deviation of the contents of a prepackage is the quantity by which the
the actual contents of the prepackage are less than the nominal quantity
the finished package.
2.4. the tolerable negative error contents of a prepackage is fixed in
accordance with the following table, in which the nominal quantity Qn
Prepackaging:
------------------------------------------------------------------
The nominal quantity Qn tolerable negative error
in grams or millilitres, as% of Qn in g or ml
------------------------------------------------------------------
from 5 to 50 9-
from 50 to 100-4.5
from 100 to 200 4.5-
from 200 to 300-9
from 300 to 500 3-
from 500 to 1 000-15
from 1 000 to 10 000 1.5-
------------------------------------------------------------------
When using the table, the values of the tolerable negative deviations of the content
listed in the table as percentages in units of weight or
the volume shall be rounded up to the nearest one tenth of a gram or millilitre.
3.
INSCRIPTIONS AND MARKINGS
All prepackages prepared according to this order shall be affixed to
on the package of the following details, which shall be irremovable,
easily legible and visible on the prepackage in normal conditions of
his presentation:
3.1 the nominal quantity (nominal weight or nominal volume)
the content expressed in kilogrammes, grammes, litres, centilitres or
millilitres, and marked in figures to be high:
3.1.1 at least 6 mm, if the nominal quantity greater than 1 000
g or 100 cl;
3.1.2 a minimum of 4 mm, if the nominal quantity equal to 1 000 g
or 100 cl or less, but greater than 200 g or 20 cl;
3.1.3 at least 3 mm high if the nominal quantity is equal to 200 g or
20 cl or less, but greater than 50 g or 5 cl;
3.1.4. at least 2 mm if it is the nominal quantity of 50 g or 5 cl
or smaller.
The nominal quantity of which is followed by the symbol for the unit of measurement
or, where appropriate, the name of the unit laid down in the specific
law ^ 3);
3.2 mark or inscription enabling the competent authority to identify
the packer or the person who ensures that the package has been properly completed,
or identify the importer;
3.3 the symbol "e" at least 3 mm high, placed in the same field
as an indication of the nominal weight or nominal volume of the contents; It
constitutes a guarantee provided by the packer or importer, that the finished
packaging meets the requirements of this order; his graphic design sets
a special law ^ 4).
4.
MEASUREMENT AND CONTROL
The quantity of product contained in a prepackage (hereinafter referred to as the "real content")
measured or checked packer or the importer using the specified
the gauge of a suitable to perform the necessary operations.
Check can be carried out on the samples taken at random
statistical collection.
In cases where the actual contents is not measured, the check must be carried out by the
organised so as to ensure that the quantity of content in an efficient manner.
This condition is fulfilled if the production control shall be carried out in
accordance with procedures accepted by the Czech metrology Institute, and if
available documents containing the results of such checks, in order to
showed that these checks with all the corrections and nastavováními, which
have proven to be necessary, have been carried out in a fair and accurate manner.
For products whose amount is stated in units of volume, the
manufacture a product in a prepackaged one of the methods for verifying that they are
the fulfilment of the requirements for the measurement and control, the use of volumetric packaging type
that is defined by specific legislation ^ 5), which covers
are fulfilled under the conditions that are specified in this Decree and in
a special law of the ^ 5).
5.
THE CHECKS THAT MUST BE CARRIED OUT AS DETERMINED BY SPECIAL LEGAL AUTHORITY
^ LAW 6) in the PREMISES of the PACKER or the IMPORTER or HIS REPRESENTATIVE
Checks to verify that the batches of finished balenívyhovují the provisions of this
the Decree, must be carried out by the competent authority in the form of statistical ^ 6)
acceptance.
Statistical inspection must be carried out in accordance with the principles used
acceptance sampling methods. The effectiveness of acceptance must be comparable with the
efficiency of the reference method specified in annex No. 2.
If this is the criterion for the minimum permitted amount shall be deemed to
the sampling plan for comparable with the sampling plan, recommended in the
Annex No. 2, if the line item of the corresponding value of 0.10
the operational characteristics of the used sampling plan (that is, for
the probability of accepting benefits straight 0.10) deviates from the straight line
the corresponding point of the operational characteristics of a sampling plan
recommended in annex No. 2 by less than 15%.
As regards the criterion for the mean value control
m
and based on the calculation of the standard deviation
with
the sampling plan shall be considered as comparable with the sampling plan
recommended in annex No. 2 If the operational
characteristics of the used sampling plan differs from the operational
the characteristics of the sampling plan recommended in annex No. 2-taking
for both operational characteristics, the axis lines applied
(Qn-m)/sec
-in point with pořadnicí 0.10 (thus the likelihood of the adoption benefits
straight 0.10) of less than 0.05.
3) Decree No. 264/2000 Coll., on the basic units of measurement and
other units and their labelling, as amended by Decree No.
424/2009 Sb.
4) Decree No. 262/2000 Coll., which ensures consistency and accuracy
measuring instruments and measurements, as amended.
5) Decree No. 331/2000 Coll. laying down requirements relating to the
bottles used as measuring containers for prepackaged goods.
6) § 9a of the law No. 505/1990 Coll. on metrology, as amended by Act No.
119/2000 Coll., Act No. 137/2002 Coll. and Act No. 155/2010 Coll.
Annex 2 to the Decree No 328/2000 Sb.
REFERENCE METHODS
This annex lays down the procedures of the reference method for the application of statistical
acceptance of batches of prepackages to verify compliance with the requirements of section
3 and point 5 of Annex No. 1.
1.
REQUIREMENTS FOR MEASURING THE ACTUAL CONTENTS OF PREPACKAGES
The actual contents of prepackages may be measured directly using the
scales or meters volume, or in the case of liquids, indirectly weighing cash
the packaged product and by measuring its density.
Regardless of the method used may not be the measurement error of the actual content
pre-packed products greater than one-fifth of the tolerable negative
tolerance for the nominal quantity in the prepackage.
2.
REQUIREMENTS FOR CHECKING BATCHES OF PREPACKAGES
The checking of prepackages shall be carried out statistical collection and must
be implemented in two parts:
and control of the actual contents) of each prepackage in the selection and
(b)) the control based on the average value of the actual contents of the finished
packaging in the selection.
A batch of prepackages shall be considered acceptable if the results of
both these checks satisfy the acceptance criteria of the relevant at the same time.
For each of these checks, there are two sampling plans:
and one for non-destructive testing), IE. testing, in which
do not open the packaging,
(b)) the other for destructive testing, i.e.,. testing, which is a wrapper
opened or destroyed.
For economic and practical reasons, the latter test shall be
limited to the absolutely essential minimum, since the effectiveness of the sampling
control in destructive testing is less than the efficiency of sampling
checks on non-destructive testing.
Therefore, the latter test shall be applied only when it is
non-destructive testing is impracticable. The general rule is
the destructive testing should not be used for benefits that include
less than 100 units.
2.1 batches of prepackages
2.1.1 Batch to be inspected must include all prepackages
of the same nominal amount, of the same type and the same production batch,
that was packaged in the same place. The batch size shall be limited to
the quantities are specified below.
2.1.2 where the prepackages are checked at the end of the packing line,
number of packages in each batch shall be equal to the maximum hourly production
the packing line, without any restrictions on the size of the dose.
In other cases the batch size shall be limited to 10 000
units.
2.1.3 at doses containing fewer than 100 prepackages, the
non-destructive testing, if implemented, be carried out
one hundred percent.
2.1.4 prior to the implementation of the tests in 2.2 and 2.3 shall be random
way to remove from a sufficient number of batches of prepackages, and such
to make check requiring the larger selection. For a different
control must be required to remove the selection at random from the first large
selection and samples must be marked.
This operation must end before marking the start of the measurement operations.
2.2 Checking the actual contents of the individual prepackages
The minimum acceptable contents shall be calculated by subtracting the tolerable negative
derogations for the tables of contents from the nominal quantity of the prepackage.
Prepackages in the batch whose actual contents are less than the minimum
acceptable content shall be considered packaging mismatch.
2.2.1. Non-destructive testing
Non-destructive testing shall be carried out in accordance with a sampling
Double plan set forth in the table below.
The number of prepackages checked shall be equal to the first selection
the range of the first selection that is specified in the sampling plan. About dose
prepackages shall be decided as follows:
2.2.1.1 charge shall for the purposes of this check, must be considered as an acceptable,
If the number of non-conforming package found in the first select is equal to
the number given in the table as the acceptance criterion or is less than the
This number;
2.2.1.2 the levy for the purposes of this check must be rejected if the number of
non-conforming package found in the first select is equal to the number given in the
the table as a rejection criterion or is larger than this number;
2.2.1.3 the dose cannot be decide after an inspection of the first selection and must be
take a second choice, if the number of non-conforming packaging identified in the first
the choice is between the number given as the acceptance criteria and the number indicated
as a rejection criterion.
Mismatched units found in the first and in the second the selection must be summed
together and provide a summary of the number of non-conforming units. About dose
prepackages shall be decided as follows:
2.2.1.4 after checking the second selection, the levy for the purposes of this check,
must be considered as acceptable if the aggregate number of non-conforming
units equal to the number given in the table as an acceptance criterion after
the second choice, or is less than this number,
2.2.1.5 after checking the second selection, the levy for the purposes of this check,
must reject, if the aggregate number of non-conforming units is equal to
the number given in the table as an opt-out after the second criterion of the selection or
is greater than this number.
------------------------------------------------------------------------------------------------
The dose range Selections Acceptance criterion Rejection criterion
prepackages order total range range (in the number of non-conforming package in the sample)
------------------------------------------------------------------------------------------------
the first 100 to 500 30 30 1 3
The other 30 60 4 5
501 to 3 200 50 50 2 5 First
The second 50 100 6 7
3 201 and more the first 80 80 3 7
The second 80 160 8 9
------------------------------------------------------------------------------------------------
2.2.2. Destructive Testing
Destructive testing shall be carried out in accordance with the
single sampling plan and should be used only for the benefits that
have 100 or more units.
The number of prepackages checked shall be 20 units. About dose
prepackages shall be decided as follows:
2.2.2.1. the levy shall be for the purpose of this inspection shall be considered as acceptable,
If the number of non-conforming units identified in the selection is equal to the number
referred to in the table as the acceptance criterion or is less than this
number;
2.2.2.2. the benefit is for the purpose of this inspection shall be rejected if the number of
non-conforming units identified in the selection is equal to the number given in the
the table as a rejection criterion or is larger than this number.
------------------------------------------------------------------------------------
The range of dose Range Acceptance criterion Rejection criterion
prepackages selection (in the number of non-conforming package in the sample)
------------------------------------------------------------------------------------
Any number of (> = 100) 20 1 2
------------------------------------------------------------------------------------
2.3 Checking the mean values of the actual contents of each of the finished
the Pack making up a batch
2.3.1 a batch of prepackages shall for the purpose of this inspection shall be considered
acceptable if the sample average
-1
x =-sum (xi) the actual contents of
XI
identified in the
n
prepackages in the selection is greater than the value of
n
With
Qn-------------t (1-Alpha)
the square root of n
In this formula is:
Qn the nominal quantity of the prepackage,
n the number of prepackages in the selection for this check,
with an estimate of the standard deviation of the actual contents of the batch,
t (1-Alpha) confidence level of 0.995 student's distribution when the degree of freedom nu = n-1.
2.3.2. If the xinaměřená value for the actual contents of the i-th unit
in a selection that contains the n units, then:
2.3.2.1 the sample average of the values measured in the selection is obtained using the
relationship:
-1 n
x =-sum (xi)
n i = 1,
2.3.2.2 and an estimate of the standard deviation of the actual contents of the batch with balenív
by using these links:
-sum of the squares of measured values:
n
sum xi2,
I = 1
-the square of the sum of the measured values:
n
(sum of xi) 2
I = 1
-and then
1 n
-(sum of xi) 2,
n i = 1
-the difference of the sum of:
n 1 n
SC = sum xi2----(sum of xi) 2,
I = 1 i = 1 n
-variance estimation the actual contents of the package in a batch:
SC
ný = ----- ,
n-1
-an estimate of the standard deviation of the actual contents of the package in a batch:
S = square root of Nu
2.3.3. Acceptance and rejection criteria for the batch of prepackages for
checking the mean:
2.3.3.1 the criteria for non-destructive testing:
+---------------------------------------------------------------------------------+
| The range of dose selection range Acceptance criterion Rejection criterion |
+---------------------------------------------------------------------------------+
| - - |
100 to 500 | (including) 30 x Qn-0.503 > = S x < Qn-0.503 S | | | |--| | > 500 50 x Qn-0.379 > = S x < Qn-0.379 S | +---------------------------------------------------------------------------------+ 2.3.3.2 Criteria for destructive testing: +---------------------------------------------------------------------------------+ dose Range Range selection | Acceptance criterion Rejection criterion | +---------------------------------------------------------------------------------+ |--| | Any number of (> = 100) 20 x > = Qn-0.640 with x Qn-0.640 with < |
+---------------------------------------------------------------------------------+
Annex No. 3 to Decree No. 328/2000 Coll.
THE PERMISSIBLE NOMINAL VOLUMES OF CERTAIN LIQUID PRODUCTS CONTAINED IN THE
PREPACKAGES
1. products SOLD by VOLUME (quantity in ml)
---------------------------------------------------------------------------------------------------------------
Silent wine on the interval from 100 ml to 1 500 ml only the following eight nominal quantities:
ml: 100-187-250-375-500-750-1 000-1 500
---------------------------------------------------------------------------------------------------------------
Yellow wine on the interval from 100 ml to 1 500 ml only this one the nominal quantity:
ml: 620
---------------------------------------------------------------------------------------------------------------
Sparkling wine on the interval from 125 ml to 1 500 ml only the following five nominal quantities:
ml: 125-200-375-750-1 500
---------------------------------------------------------------------------------------------------------------
Liqueur wine on the interval from 100 ml to 1 500 ml only the following seven nominal quantities:
ml: 100-200-375-500-750-1 000-1 500
---------------------------------------------------------------------------------------------------------------
-In the range from 100 ml to 1 500 ml only the following seven nominal quantities:
wine 100 ml-200-375-500-750-1 000-1 500
---------------------------------------------------------------------------------------------------------------
Spirits on the interval from 100 ml to 2 000 ml only the following nine jmenovitýchmnožství:
ml: 100 — 200 — 350 — 500 — 700 — 1 000-1 500-1 750-2 000
---------------------------------------------------------------------------------------------------------------
2. PRODUCT DEFINITION
---------------------------------------------------------------------------------------------------------------
Silent wine wine, as defined in the applicable legislation of the European Union directly ^ 7) and referred to under code nomenclature
Within CN code ex 2204 in directly applicable legislation the European Union ^ 8).
---------------------------------------------------------------------------------------------------------------
Yellow wine wine, as defined in the applicable legislation of the European Union directly to ^ 9), referred to under code nomenclature
Within CN code ex 2204 in directly applicable legislation the European Union ^ 8) and with designation of origin: "Côtes du Jura",
"Arbois", "L ' Étoile" and "Château-Chalon" in bottles as defined in applicable legislation directly
The European Union ^ 10).
---------------------------------------------------------------------------------------------------------------
Sparkling wine wine, as defined in the applicable legislation of the European Union directly ^ 11) under the number auvedené 2204 10
directly applicable legislation in the European Union ^ 8).
---------------------------------------------------------------------------------------------------------------
Liqueur wine Wine, as defined in the applicable legislation of the European Union directly ^ 12) auvedené under the number 2204 21
directly applicable to 2204 29 in respect of the European Union ^ 8).
---------------------------------------------------------------------------------------------------------------
Egg-based aromatized wine, as defined in the applicable legislation of the European Union directly ^ 13) and referred to
wine under the number 2205 in European Union legislation directly applicable ^ 8).
---------------------------------------------------------------------------------------------------------------
Spirit drinks spirit drinks as defined in the applicable legislation of the European Union directly ^ 14) and listed under the
number of directly applicable provisions in 2208 European Union ^ 8).
---------------------------------------------------------------------------------------------------------------".
7) Article. 1 (1). 2 (a). b) Council Regulation (EC) No 1493/1999 of 17 May.
May 1999 on the common organisation of the market in wine.
8) Council Regulation (EEC) No 2658/87 of 23 December 2003. July 1987 on the tariff and
statistical nomenclature and on the common customs tariff.
9) Article. 1 (1). 2 (a). b) Council Regulation (EC) No 1493/1999 of 17 May.
May 1999 on the common organisation of the market in wine.
10) point 3 of annex I to Commission Regulation (EC) No 753/2002 of 29 September 2003. April
2002 laying down certain detailed rules for the application of Council Regulation (EC)
No 1493/1999 to the description, designation, presentation and protection of certain
wine products.
11) Article. 1 (1). 2 (a). (b)), and paragraphs 15 to 18 of annex I to Regulation (EC) No.
1493/1999.
12) Article. 1 (1). 2 (a). (b)) and paragraph 14 of annex I to Regulation (EC) No.
1493/1999.
13) Article. 2 (2). 1 (b). and) Council Regulation (EEC) No 1601/91 of 10 June 1999.
June 1991 laying down general rules on the definition, description
and presentation of aromatized wines, aromatized wine-based drinks and
aromatized wine-product cocktails, as amended by the Act of accession of
2005.
14) Article. 2 (2). 1 European Parliament and Council Regulation (EC) No.
110/2008 of 15 March. January 2008 on the definition, description, presentation,
labelling and protection of geographical indications of spirit drinks and repealing Regulation
Council Regulation (EEC) No 1576/89.
Article. (II)
The effectiveness of the
This Decree shall take effect on the date of 15. September 2012.
Minister:
Mudr. Cuba in r.