Potrebujeme váš súhlas na využitie jednotlivých dát, aby sa vám okrem iného mohli ukazovať informácie týkajúce sa vašich záujmov. Súhlas udelíte kliknutím na tlačidlo „OK“.
Standard Specification for Polysulfone Resin for Medical Applications
Automaticky preložený názov:
Štandardné špecifikácie pre polysulfónu živice pre lekárske aplikácie
NORMA vydaná dňa 1.9.2010
Označenie normy: ASTM F702-10
Poznámka: NEPLATNÁ
Dátum vydania normy: 1.9.2010
Kód tovaru: NS-56168
Počet strán: 4
Približná hmotnosť: 12 g (0.03 libier)
Krajina: Americká technická norma
Kategória: Technické normy ASTM
Ostatní normy týkající se laboratorního lékařství
Termoplasty
Keywords:
plastic surgical devices/applications, polymerssurgical applications, polysulfone resins , unfilled polysulfone (PSU), Plastic surgical devices/applications--specifications, Polymers (surgical applications)--specifications, Polysulfone resins, Surgical implant resins--specifications, Surgical implants--specifications, Thermoplastic surgical implant applications--specifications, ICS Number Code 11.100.99 (Other standards related to laboratory medicine), 83.080.20 (Thermoplastic materials)
1. Scope | ||||||||||||
1.1 This specification covers polysulfone resin (poly(oxy-1,4-phenylenesulfonyl-1,4–phenylene (dimethylmethylene)-1,4–phenylene)) as defined in ISO 25137–1, supplied by a vendor in virgin form (pellets, powder, fabricated forms and so forth) for medical applications. This specification provides requirements and associated test methods for this thermoplastic when it is intended for use in manufacturing medical devices or components of medical devices. 1.2 As with any material, some characteristics may be altered by the processing techniques (such as molding, extrusion, machining, sterilization, and so forth) required for the production of a specific part or device. Therefore, properties of fabricated forms of this resin should be evaluated using test methods which are appropriate to ensure safety and efficacy as agreed upon by the vendor, purchaser, and regulating bodies. 1.3 The standard allows for designation of polysulfone resin for all medical applications. The actual extent of performance and suitability for a specific application must be evaluated by the vendor, purchaser, and regulating bodies. 1.4 The properties included in this specification are those applicable for unfilled polysulfone (PSU) polymers with the addition of colorants and processing aids. Indicated properties are for injection molded forms. Forms containing fillers or other additives, as well as polymer blends which contain PSU, or reclaimed materials, are not covered by this specification. 1.5 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard. 1.6 When evaluating material in accordance with this specification, hazardous materials, operations, and equipment may be involved. This standard does not purport to address all of the concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety and health practices and determine the applicability of regulatory limitations prior to use. |
||||||||||||
2. Referenced Documents | ||||||||||||
|
Historická
15.4.2010
Historická
1.1.2008
Historická
1.11.2013
Historická
1.3.2014
Historická
1.8.2009
Historická
1.8.2009
Posledná aktualizácia: 2024-12-22 (Počet položiek: 2 217 000)
© Copyright 2024 NORMSERVIS s.r.o.