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DIN 13097-4:2009-08

Superseded

Superseded

A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.

View Superseded by

HYPODERMIC NEEDLES - PART 4: POINT GEOMETRY, REQUIREMENTS AND TESTING

Available format(s)

Hardcopy , PDF

Superseded date

03-06-2019

Superseded by

DIN 13097-4:2019-06

Language(s)

German

Published date

01-01-2009

€72.80
Excluding VAT

Vorwort
Einleitung
1 Anwendungsbereich
2 Normative Verweisungen
3 Begriffe
4 Masse, Bezeichnungen
  4.1 Rohrabmessungen
  4.2 Anschliffarten
5 Werkstoff
6 Anforderungen
  6.1 Kanüle
  6.2 Montageseitiges Ende der Rohkanüle
  6.3 Eigenschaften des Schliffes
  6.4 Sauberkeit
  6.5 Verpackung
  6.6 Transport und Lagerung
Anhang A (informativ) - Medizinische Kanülen - Abmessungen
Anhang B (informativ) - Masse für Schliff A (Facettenschliff)
         - Schliffausführung für ultralangen, langen, mittleren
         und kurzen Facettenschliff
Anhang C (normativ) - Fragmentationsprüfung für medizinische
         Kanülen
Anhang D (normativ) - Penetrationsprüfung
Anhang E (informativ) - Anmerkung zu Kanülen-Gauge oder
         Needle-Gauge
Literaturhinweise
Bilder
Tabellen

This standard is included in DIN Handbook 463.

DevelopmentNote
Supersedes DIN 13097. (08/2009) DRAFT 2018 issued in April 2018. (04/2018)
DocumentType
Standard
Pages
20
PublisherName
German Institute for Standardisation (Deutsches Institut für Normung)
Status
Superseded
SupersededBy
Supersedes

DIN HDBK 463 : 3ED 2014 MEDIZINISCHE GERAETE UND BEHAELTNISSE FUER TRANSFUSION, INFUSION UND INJEKTION
UNI EN ISO 22413 : 2013 TRANSFER SETS FOR PHARMACEUTICAL PREPARATIONS - REQUIREMENTS AND TEST METHODS
EN ISO 22413:2013 Transfer sets for pharmaceutical preparations - Requirements and test methods (ISO 22413:2010)
I.S. EN ISO 22413:2013 TRANSFER SETS FOR PHARMACEUTICAL PREPARATIONS - REQUIREMENTS AND TEST METHODS (ISO 22413:2010)
UNE-EN ISO 1135-3:2017 Transfusion equipment for medical use - Part 3: Blood-taking sets for single use (ISO 1135-3:2016)
DIN EN ISO 1135-3:2017-05 TRANSFUSION EQUIPMENT FOR MEDICAL USE - PART 3: BLOOD-TAKING SETS FOR SINGLE USE (ISO 1135-3:2016)
DIN EN ISO 22413:2013-10 Transfer sets for pharmaceutical preparations - Requirements and test methods (ISO 22413:2010)
I.S. EN ISO 1135-3:2017 TRANSFUSION EQUIPMENT FOR MEDICAL USE - PART 3: BLOOD-TAKING SETS FOR SINGLE USE (ISO 1135-3:2016)
UNE-EN ISO 22413:2013 Transfer sets for pharmaceutical preparations - Requirements and test methods (ISO 22413:2010)
BS ISO 11040-4:2015 Prefilled syringes Glass barrels for injectables and sterilized subassembled syringes ready for filling
DIN EN ISO 1135-3 E : 2017 TRANSFUSION EQUIPMENT FOR MEDICAL USE - PART 3: BLOOD-TAKING SETS FOR SINGLE USE (ISO 1135-3:2016)
13/30273499 DC : 0 BS ISO 11040-4 - PREFILLED SYRINGES - PART 4: GLASS BARRELS FOR INJECTABLES AND STERILIZED SUBASSEMBLED SYRINGES READY FOR FILLING
BS EN ISO 22413:2013 Transfer sets for pharmaceutical preparations. Requirements and test methods
ISO 11040-4:2015 Prefilled syringes — Part 4: Glass barrels for injectables and sterilized subassembled syringes ready for filling
ISO 1135-3:2016 Transfusion equipment for medical use Part 3: Blood-taking sets for single use
EN ISO 1135-3:2017 Transfusion equipment for medical use - Part 3: Blood-taking sets for single use (ISO 1135-3:2016)
BS EN ISO 1135-3:2017 Transfusion equipment for medical use Blood-taking sets for single use
DIN EN ISO 1135-3:2014-12 (Draft) TRANSFUSION EQUIPMENT FOR MEDICAL USE - PART 3: BLOOD-TAKING SETS FOR SINGLE USE (ISO 1135-3:2016)
DIN ISO 11040-4:2007-10 PREFILLED SYRINGES - PART 4: GLASS BARRELS FOR INJECTABLES AND STERILIZED SUBASSEMBLED SYRINGES READY FOR FILLING (ISO 11040-4:2015)
BS ISO 22413:2010 Transfer sets for pharmaceutical preparations. Requirements and test methods
ISO 22413:2010 Transfer sets for pharmaceutical preparations Requirements and test methods
DIN ISO 11040-4:2017-07 PREFILLED SYRINGES - PART 4: GLASS BARRELS FOR INJECTABLES AND STERILIZED SUBASSEMBLED SYRINGES READY FOR FILLING (ISO 11040-4:2015)

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