C08 标志、包装、运输、贮存 标准查询与下载



共找到 343 条与 标志、包装、运输、贮存 相关的标准,共 23

Packaging for terminally sterilized medical devices. Sterilization wrap. Requirements and test methods

ICS
11.080.30;55.040
CCS
C08
发布
2017-02-28
实施
2017-02-28

Packaging for terminally sterilized medical devices. Paper for use in the manufacture of paper bags (specified in EN 868-4) and in the manufacture of pouches and reels (specified in EN 868-5). Requirements and test methods

ICS
11.080.30;55.040
CCS
C08
发布
2017-02-28
实施
2017-02-28

Packaging for terminally sterilized medical devices. Paper for low temperature sterilization processes. Requirements and test methods

ICS
11.080.30;55.040
CCS
C08
发布
2017-02-28
实施
2017-02-28

Packaging for terminally sterilized medical devices. Paper bags. Requirements and test methods

ICS
11.080.30;55.040;55.080
CCS
C08
发布
2017-02-28
实施
2017-02-28

Containers and accessories for pharmaceutical preparations - Part 7: Screw-neck vials made of glass tubing for liquid dosage forms (ISO 11418-7:2016)

ICS
11.040.20;11.120.99
CCS
C08
发布
2017-02
实施

Containers and accessories for pharmaceutical preparations - Part 5: Dropper assemblies (ISO 11418-5:2015)

ICS
11.120.99;55.100
CCS
C08
发布
2017-02
实施

Medical devices - Symbols to be used with medical device labels, labelling and information to be supplied - Part 1: General requirements

ICS
01.080.20;11.040.01
CCS
C08
发布
2016-11-01
实施

Plastic collapsible containers for human blood and blood components

ICS
11.040.20
CCS
C08
发布
2016-10-01
实施

This European Standard specifies performance requirements and methods of test for non-reclosable packaging that have been designated child-resistant. This European Standard is intended for type approval only and is not intended for quality assurance purposes.

Child-resistant non-reclosable packaging for pharmaceutical products - Requirements and testing

ICS
11.120.99;55.020;97.190
CCS
C08
发布
2016-07
实施

Primary packaging materials for medicinal products. Particular requirements for the application of ISO 9001:2008, with reference to Good Manufacturing Practice (GMP)

ICS
03.120.10;11.040.01
CCS
C08
发布
2015-11-30
实施
2015-11-30

Primary packaging materials for medicinal products - Particular requirements for the application of ISO 9001:2008, with reference to Good Manufacturing Practice (GMP)

ICS
03.120.10;11.040.01;11.120.10;55.040
CCS
C08
发布
2015-10
实施

Packaging for terminally sterilized medical devices - Part 1: Requirements for materials, sterile barrier systems and packaging systems (ISO 11607-1:2006 + Amd 1:2014); German version EN ISO 11607-1:2009 + A1:2014

ICS
11.080.30
CCS
C08
发布
2014-11-01
实施

Packaging. Braille on packaging for medicinal products

ICS
11.120.99;11.180.30;55.020
CCS
C08
发布
2014-10-31
实施
2014-10-31

La présente Norme internationale spécifie les exigences et fournit les lignes directrices relatives à l'application du braille sur l'étiquetage des médicaments.

Packaging - Braille on packaging for medicinal products

ICS
11.120.99;11.180.30;55.020
CCS
C08
发布
2014-10-03
实施
2014-10-03

Packaging - Braille on packaging for medicinal products (ISO 17351:2013); German version EN ISO 17351:2014

ICS
11.180.30;55.020
CCS
C08
发布
2014-10-01
实施

Transfer sets for pharmaceutical preparations - Requirements and test methods

ICS
11.120.99
CCS
C08
发布
2013-08-31
实施
2013-08-31

This part of ISO 3826 specifies requirements, including performance requirements, for plastics collapsible, non-vented, sterile containers complete with collecting tube outlet port(s), integral needle, and with optional transfer tube(s), for the collection, storage, processing, transport, separation, and administration of blood and blood components. The plastics containers may contain anticoagulant and/or preservative solutions, depending on the application envisaged.

Plastics collapsible containers for human blood and blood components.Part 1: Conventional containers

ICS
11.040.20
CCS
C08
发布
2013-06
实施

Dosage specifications and color codes of small packages of traditional Chinese medicine decoction pieces

ICS
11.120.99
CCS
C08
发布
2013-05-21
实施
2013-09-01

(a) Live poultry. All live poultry, except eggs for hatching, offered for importation from any region of the world shall be accompanied by a certificate stating that such poultry and their flock or flocks of origin were inspected on the premises of origin immediately before the date of movement from such region and that they were then found to be free of evidence of communicable diseases of poultry. The certificate shall also state that, as far as it has been possible to determine, during the 90 days prior to movement, the poultry were not exposed to communicable diseases of poultry and the premises were not in any area under quarantine. The certificate shall also state that the poultry have not been vaccinated with a vaccine for the H5 or H7 subtype of avian influenza. The certificate shall also state that the poultry have been kept in the region from which they are offered for importation since they were hatched, or for at least 90 days immediately preceding the date of movement, that the poultry have not been moved through a region identified in accordance with § 94.6(a) of this subchapter as a region where any form of highly pathogenic avian influenza exists, and that, as far as it has been possible to determine, nocase of highly pathogenic avian influenza or Newcastle disease occurred on the premises where such poultry were kept, or on adjoining premises, during that 90-day period.

Animals and Animal Products. Part93:Importation of certain animals,birds,fish,and poultry,and certain animal,bird,and poultry products; requirements for means of conveyance and shipping containers. Section93.205:Certificate for live poultry and hatc

ICS
CCS
C08
发布
2013-03-29
实施
2013-03-29

Medical devices - Symbols to be used with medical device labels, labelling and information to be supplied - Part 1: General requirements (ISO 15223-1:2012); German version EN ISO 15223-1:2012, with CD-ROM

ICS
01.080.20;11.040.01
CCS
C08
发布
2013-02
实施



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