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 Guide for Evaluation of Thermoplastic Polyurethane Solids and Solutions for Biomedical Applications (Includes all amendments And changes 8/16/2017).
Automaticky preložený názov:
Štandardné Príručka pre hodnotenie z termoplastického polyuretánu , pevných látok a riešení pre biomedicínske aplikácie
NORMA vydaná dňa 10.10.1998
Označenie normy: ASTM F624-98ae1
Poznámka: NEPLATNÁ
Dátum vydania normy: 10.10.1998
Kód tovaru: NS-55939
Počet strán: 4
Približná hmotnosť: 12 g (0.03 libier)
Krajina: Americká technická norma
Kategória: Technické normy ASTM
Keywords:
plastic surgical devices/applications, polymers-surgical applications, polyurethane-medical applications
1. Scope | ||||||||||||||||||||||||||||||||||||||||||||||||
1.1 This guide covers the evaluation of thermoplastic polyurethanes in both solid and solution form for biomedical applications. The polymers have been reacted to completion and require no further chemical processing. 1.2 The tests and methods listed in this guide may be referenced in specification containing minimum required values and tolerances for specific end use products. 1.3 Test values shall be stated in SI units with inch-pound units in parentheses. 1.4 Standard tests for biocompatibility are included to aid in the assessment of safe utilization in biomedical applications. Compliance with these criteria shall not be constructed as an endorsement of implantability. Since many compositions, formulations, and forms of thermoplastic polyurethanes in solid and solution forms are within this material class, the formulator or fabricator must evaluate the biocompatibility of the specific composition or form in the intended use and after completion of all manufacturing processes including sterilization. 1.5 Purchase specifications may be prepared by agreement between the buyer and seller by selection of appropriate tests and methods from those listed applicable to the specific biomedical end use. 1.6 This standard does not purport to address all of the safety 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 | ||||||||||||||||||||||||||||||||||||||||||||||||
|
Chcete mať istotu o platnosti využívaných predpisov?
Ponúkame Vám riešenie, aby ste mohli používať stále platné (aktuálne) legislatívne predpisy
Chcete vedieť viac informácií ? Pozrite sa na túto stránku.
Posledná aktualizácia: 2025-07-11 (Počet položiek: 2 208 012)
© Copyright 2025 NORMSERVIS s.r.o.