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TECHNICAL DATA SHEET

BD Plastipak™ syringes without needles and
BD General Syringes without needle
Sterile, Single Use, Latex free

1. General Information

1.1 General
BD Plastipak™ syringes are used for general purpose injection and aspiration of fluids from vials,
ampoules and parts of the body below the surface of the skin. Perfusion syringes, 50ml syringes,
are designed for short term use in syringe pumps (active IIa devices) for the administration of
pharmaceuticals. The 50 ml Catheter Tip Syringes have a long tapered tip designed to aid in
irrigation or for connection to non-ISO compatible Luer connections such as nasogastric tubes.

DEAD SPACE (maximum, without needle) (except for catheter tip syringes)
SYRINGE SIZE 1 ml 2ml 5ml 10ml 20ml 30ml 50ml 100ml
Dead Space 0.07 ml 0.07ml 0.075ml 0.10ml 0.15ml 0.17ml 0.20ml 0.20ml
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LUER SLIP SYRINGES

Reference Capacity Description Scale Graduation Box (units) Case (units)
300026 1 ml Insulin 40 I.U. International units 100 800
301355 1 ml Insulin 100 I.U. International units 100 800
303174 1 ml Insulin 100 I.U. International units 120 960
303173 1 ml Insulin 40 I.U. International units 120 960
300013 1 ml Central cone 0.01 ml 100 800
303172 1 ml Central cone 0.01 ml 120 960
300185 2/ 2.5 ml Central cone 0.1 ml 100 800
302187 5 ml Central cone 0.2 ml 100 400
302188 10 ml Eccentric cone 0.5 ml 100 400
301183 20 ml Eccentric cone 1 ml 60 240
300613 20 ml Eccentric cone 1 ml 120 480
301231 30 ml Eccentric cone 1 ml 60 240
300866 50/ 60 ml Eccentric cone 1 ml 60 240
300867 50/ 60 ml Catheter tip 1 ml 60 240
300605 100 ml Catheter tip with Luer adaptor 2 ml 25 50
309654 60ml Slip tip 1 ml 40 160

LUER LOK™ SYRINGES

Reference Capacity Description Scale Graduation Box (units) Case (units)
301189 20 ml Luer Lok™ 1 ml 60 240
300629 20 ml Luer Lok™ 1 ml 120 480
301229 30 ml Luer Lok™ 1 ml 60 240
300865 50/60 ml Luer Lok™ 1 ml 60 240
300137 50 ml Luer Lok™ Perfusion 1 ml 50 100
300139 50 ml Luer Lok™ Perfusion Amber 1 ml 50 100
309653 60ml Luer Lok™ 1 ml 40 160
309628 1 ml Luer Lok™ 0.01 ml 100 800
309658 3ml Luer Lok™ 0.1ml 200 800
309649 5ml Luer Lok™ 0.2ml 125 500
300912 10ml Luer Lok™ 0.2ml 100 400
305959* 10ml Luer Lok™ 0.2ml 100 400
300869 50/ 60 ml Luer Lok™ AMBER 1 ml 60 240
*305959 will be preferred to supply to European customers as this catalogue number of 10ml Luer Lok™ Plastipak
is manufactured in Europe.

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1.2 Certification
BD BD ISO CE MARKING BD MANUFACTURING
REFERENCE MANUFACTURER CERTIFICATION SITE
301189 Becton Dickinson & NSAI - Certificate NSAI NB no Becton Dickinson S.A. -
301183 Company Limited MD 19.1609 I.S. EN 0050: Certifícate Camino de Valdeoliva, s/n.
300629 Donore Road ISO 13485:2012 N° 252.156 28750, San Agustin del
301229 Drogheda Guadalix (Madrid) Spain
300865 Co. Louth
300869 Ireland
300867
300605
300613
301231
300866
300137
300139
300026 Becton Dickinson AENOR –N. ER- AEMPS 0318: Becton Dickinson S.A. -
301355 S.A. - Camino de 0264/1994 – ISO Certifícate N° Camino de Valdeoliva, s/n.
300013 Valdeoliva, s/n. 9001:2008; 2000 06 0273 28750, San Agustin del
300185 28750, San Agustin CP Guadalix (Madrid) Spain
302187 del Guadalix (Madrid) AEMPS N. 2012 07
302188 Spain 0013 EN - EN – ISO
303172 13485:2013
303173
303174
305959
309628* Becton, Dickinson NSAI - ISO NSAI 0050: Becton, Dickinson and
309658 and Company 9001 :20008 Certifícate N° Company
309649 1 Becton Drive Certificate 252.231 Route 7 & Grace Way,
300910 Franklin Lakes, NJ MD19.2305 Canaan CT 06018
300911 07417, USA USA
300912 NSAI ISO
309653 13485 :2012
309654 Certificate
MD19.2305
*Catalogue number 309628 used to be manufactured in BD Singapore Branch, 30 Tuas Avenue 2, Singapore 639461.
No changes to form, fit or function when transferred to BD Canaan.

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1.3 Material
COMPONENT MATERIAL
SYRINGE
Barrels, plunger rods POLYPROPYLENE
Barrel cat# 309628 POLYCARBONATE
Stoppers LATEX FREE ELASTOMER
2
Lubricant MEDICAL GRADE SILICONE OIL, <0.25 mg/cm
AMBER syringes have the barrel colored to reduce U.V. light; for administration of light sensitive medications

PACKAGING
Web packaging POLYAMIDE/POLYETHYLENE, PAPER WITH MEDICAL GRADE
Ink Printing Ink
Box HARD PAPER

1.4 Material of concern

Materials of concern are chemicals or substances that have been identified as having the potential
to cause long term effects on humans or the environment.
MATERIAL COMMENT
Phthalates The products do not contain phthalates in general and as such the products do not contain
di (2ethylhexyl) phthalate DEHP as CAS number 117-81-7, EC number 204-211-0.
Latex The products do not contain natural latex.
Bisphenol A The products do not contain Bisphenol A.
Catalogue number 309628 contain polycarbonate and hence Bisphenol A
Substances of animal The products do use industrial raw materials which contain small amounts of tallow or
origin BSE/TSE tallow derivatives (e.g. stearates in polymers). Such substances are not considered as
derivatives of animal tissues for the purpose of this rule (EU regulation 722/2012) which
therefore does not apply
Polyvinyl chloride (PVC) The products do not contain polyvinyl chloride

1.5 REACH information

Based on information available and BD’s continuous data collection efforts throughout the supply
chain, BD have not identified any chemicals in the articles and packaging with the Product
Numbers as referenced above, in an individual concentration above 0.1% weight by weight
(w/w), which have been listed as SVHC and included in the "Candidate List" published by the
European Chemical Agency (ECHA. The substances published in such list are candidates for
eventual inclusion in the List of Substances Subject to Authorization (Annex XIV of REACH).

1.6 Biocompatibility
BD Medical products comply with the requirements of the standard for biocompatibility of
medical devices, ISO 10993-1 Biological Evaluation of Medical Devices - Part 1: Evaluation and
Testing.

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1.7 Sterilization
 Ethylene Oxide Sterilization following EN ISO 11135-1. ETO residues are within
applicable regulations. All references except references below are sterilized with EO
 Radiation Sterilization following EN ISO 11137-1 References sterilized with radiation:
309628, 309658, 309649, 300910, 300911, 300912, 309653 and 309654.

1.8 Shelf life

Shelf life 5 years
No special storage or transportation condition. Recommendations to store in room temperature.
Store in dry and warm place and not exposed to strong light.

1.9 Standards
HARMONISED STANDARDS
Sterilisation of Medical Devices – requirements for medical devices to be labelled
EN 556-1:2001/ AC:2006
“sterile”.
EN 980: 2008 Graphical Symbols for use in the labelling of medical devices.
Terminology, symbols and information provided with medical devices. Information
BS EN 1041+A1: 2013
supplied by the manufacturer with medical devices
Conical fittings with a 6 % (Luer) taper for syringes, needles and certain other medical
EN 1707:1996
equipment - Lock fittings
EN 20594- Conical fittings with a 6% (Luer) taper for syringes, needles and certain other medical
1:1993/AC:1996 equipment - Part 1: General requirements
EN IS010993-series Biological evaluation of medical devices
Sterilization of health care products - Ethylene oxide - Part 1: Requirements for
EN ISO 11135-1:2007 development, validation and routine control of a sterilization process for medical
devices
EN ISO 11137-1 Sterilization of health care products - Radiation. Part1.Requirements for development,
validation and routine control of sterilization process for medical devices
EN ISO 11137-2 Sterilization of health care products – Radiation. Part2. Establishing the sterilization
dose
EN ISO 11138-2:2009 Sterilization of health care products - Biological indicators - Part 2: Biological indicators
for ethylene oxide sterilization processes
Packaging for terminally sterilized medical devices - Part 1: Requirements for
EN ISO 11607-1:2009
materials, sterile barrier systems and packaging systems
Packaging for terminally sterilized medical devices - Part 2: Validation requirements for
EN ISO 11607-2:2006
forming, sealing and assembly processes
EN ISO 11737-
Sterilization of medical devices - Microbiological methods - Part 1: Determination of a
1:2006/AC:2009
population of microorganisms on products
Sterilization of medical devices - Microbiological methods - Part 2: Tests of sterility
EN ISO 11737-2:2009
performed in the definition, validation and maintenance of a sterilization process (ISO
11737-2:2009)

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Plastipak syringes without needles TDS version March 2016

HARMONISED STANDARDS, continue
EN ISO
Medical devices – Quality management Systems Requirements for Regulatory
13485:2012/AC:2012
Purposes
EN ISO 14155:2011 Clinical investigation of medical devices for human subjects - Good clinical practice
EN ISO 14971:2012 Medical Devices. Application of risk management to medical devices
NON HARMONISED STANDARD
IS EN ISO 7864-1: 1996 Sterile hypodermic needles For Single Use
IS EN ISO 7886-1:1998 Sterile hypodermic syringes For Single use - Part 1:Syringes for manual use
Sterile Hypodermic Syringes for Single Use. Part 2: Syringes for Use with Power-
EN ISO 7886-2:1998 Driven Syringe Pumps.
See notes 2 and 3 below
Conical fittings with a 6% (Luer) taper for syringes, needles and certain other medical
ISO 594-1:1993
equipment - Part 1: General requirements
Conical fittings with 6 % (Luer) taper for syringes, needles and certain other medical
ISO 594-2:1998
equipment -- Part 2: Lock fittings
ISO 9626: 1995 Stainless steel needle tubing for the manufacture of medical devices
Medical devices – Quality management Systems Requirements for Regulatory
ISO 13485:2003
Purposes
Cleanrooms and associated controlled environments Part 1: Classification of air
ISO 14644-1:1999
cleanliness
Sterilisation of Medical Devices – requirements for medical devices to be labelled
ISO 15223-1:2012
“sterile”.
ISO 10993-2:2009 Biological Evaluation of Medical Devices Part 2
Biological evaluation of medical devices - Part 10: Tests for irritation and delayed-
ISO10993-10:2009
type hypersensitivity
Sampling procedures for inspection by attributes -- Part 1: Sampling schemes
ISO 2859-1:1999
indexed by acceptance quality limit (AQL) for lot-by-lot inspection

INSULIN GRADUATED SYRINGE ALSO MEETS ISO 8537 Sterile single-use syringes, with or without
needle, for insulin

1.10 Classification
 Class I Sterile with a measuring function (syringes from 1 to 10 ml) Medical Device
under Rule 2, Annex IX of Medical Devices Directive 93/42/EEC as amended.
 Class IIa (syringes from 20 to 50 ml) Medical Device under Rule 2, Annex V and VII IX
of Medical Devices Directive 93/42/EEC as amended.

1.11 GMDN code

GMDN code 47017: General purpose syringes.

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1.12 Good Manufacturing practices
The entire manufacturing and testing processes are following the Good Manufacturing Practices
as specified below
 Incoming raw materials are verified via material inspection and testing and our suppliers
are approved via our vendor management system.
 In addition to the automatic on-line inspections, in-process inspections are performed in
addition to final product testing to ensure compliance with approved specifications.
 The manufacturing and testing details of each batch of product are recorded on a batch
record which is retained in accordance with our document control procedures
 BD operates a system of Internal and external audits to maintain compliance
 BD confirms that it will continue to adhere to relevant international standards in designing
and manufacturing its products.
 BD reserves the right to use the internal change control procedure to change raw material
suppliers and production process

1.13 Others
 The EU representative, for syringes which BD Manufacturer is Becton, Dickinson and
Company, 1 Becton Drive, Franklin Lakes, NJ 07417, USA, is Becton Dickinson
Distribution Center, Laagstraat 57, B-9140 Temse -Belgium. Other syringes are produced
by a European manufacturer.
 (Material) Safety Data Sheets are not required for this product
 Certificate of Food Contact (COMMISSION REGULATION (EU) No. 10/2011 of January
14th, 2011 concerning materials and plastic objects intended to get in touch with
foodstuffs) is not required as BD products are used for general purpose injection and
aspiration of fluids from vials, ampoules and parts of the body below the surface of the
skin.

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2. Packaging

2.1 Packaging material

LABELS: according to European Medical Device directive, multilingual

2.2 Example labeling

Legal Manufacturer and manufacturing site: San Agustin del Guadalix

Example Unit pack cat.no 301355

Example Shelf box label cat.no 301355

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Shelf box graphics

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Plastipak syringes without needles TDS version March 2016

Legal Manufacturer: Drogheda/ Manufacturing site San Agustin del Guadalix

Example Unit pack cat.no 300867

Example Shelf box label cat.no 300867

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Shelf box graphics

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Plastipak syringes without needles TDS version March 2016

Legal Manufacturer: Franklin Lakes, Manufacturing site Canaan

Example Unit pack cat.no 309628

Exmaple Shelf box label cat.no 309628

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Shelf box graphics

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