10/30216808 DC : 0
Superseded
A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.
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BS ISO 11040-3 - PREFILLED SYRINGES - PART 3: SEALS FOR DENTAL LOCAL ANAESTHETIC CARTRIDGES
Hardcopy , PDF
29-02-2012
English
Foreword
Introduction
1 Scope
2 Normative references
3 Classification
4 Shape and dimensions
5 Designation
6 Material
7 Requirements
8 Labelling
Annex A (normative) - Leakage test
Bibliography
Committee |
CH/212
|
DocumentType |
Draft
|
Pages |
14
|
PublisherName |
British Standards Institution
|
Status |
Superseded
|
SupersededBy |
ISO 11040-2:2011 | Prefilled syringes Part 2: Plunger stoppers for dental local anaesthetic cartridges |
ISO 8871-1:2003 | Elastomeric parts for parenterals and for devices for pharmaceutical use — Part 1: Extractables in aqueous autoclavates |
ISO 7885:2010 | Dentistry Sterile injection needles for single use |
ISO 7619-1:2010 | Rubber, vulcanized or thermoplastic Determination of indentation hardness Part 1: Durometer method (Shore hardness) |
ISO 2230:2002 | Rubber products — Guidelines for storage |
ISO 9997:1999 | Dental cartridge syringes |
ISO 8872:2003 | Aluminium caps for transfusion, infusion and injection bottles — General requirements and test methods |
ISO 15378:2017 | Primary packaging materials for medicinal products — Particular requirements for the application of ISO 9001:2015, with reference to good manufacturing practice (GMP) |
ISO 13926-2:2011 | Pen systems Part 2: Plunger stoppers for pen-injectors for medical use |
ISO 8871-5:2016 | Elastomeric parts for parenterals and for devices for pharmaceutical use — Part 5: Functional requirements and testing |
ISO 11499:2014 | Dentistry — Single-use cartridges for local anaesthetics |
ISO 48:2010 | Rubber, vulcanized or thermoplastic Determination of hardness (hardness between 10 IRHD and 100 IRHD) |
ISO 11040-1:2015 | Prefilled syringes Part 1: Glass cylinders for dental local anaesthetic cartridges |
ISO 8871-4:2006 | Elastomeric parts for parenterals and for devices for pharmaceutical use Part 4: Biological requirements and test methods |
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