Standard Specification for Poly(glycolide) and Poly(glycolide-co-lactide) Resins for Surgical Implants with Mole Fractions Greater Than or Equal to 70 % Glycolide not-eligible and tickets for parking lot

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NOTE 1 The device that is commonly referred to as an active implantable medical device can in fact be a single device

• Initiation and early growth

and VSWR of connectors is useful for:

This document specifies the methods of preparation of test specimens and the standard test methods to be used in determining the properties of thermoplastic polyketone moulding and extrusion materials

Standard Specification for Poly(glycolide) and Poly(glycolide-co-lactide) Resins for Surgical Implants with Mole Fractions Greater Than or Equal to 70 % Glycolide not-eligible and tickets for parking lot1 Scope 1. 1 This specification covers both virgin poly(glycolide) homopolymer and poly(glycolide co lactide) copolymer resins intended for use in surgical implants. The poly(glycolide colactide) copolymers covered by this specification possess nominal mole fractions greater than or equal to 70 % glycolide (65. 3 % in mass fraction). This specification is also applicable to lactide co glycolide copolymers that possess glycolide segments sufficient in