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Doplňujúce informácie

ASTM F648-14

Standard Specification for Ultra-High-Molecular-Weight Polyethylene Powder and Fabricated Form for Surgical Implants

Automaticky preložený názov:

Štandard Specification pre Dyneema Prášok a umelo vytvorené pre chirurgických implantátov

NORMA vydaná dňa 1.3.2014

Jazyk
Prevedenie	PDF - okamžité stiahnutie - 79.90 € Tlačené - 79.90 €
Dostupnosť	SKLADOM
Cena	79.90 € bez DPH
79.90 €

Informácie o norme:

Označenie normy: ASTM F648-14
Poznámka: NEPLATNÁ
Dátum vydania normy: 1.3.2014
Kód tovaru: NS-56009
Počet strán: 8
Približná hmotnosť: 24 g (0.05 libier)
Krajina: Americká technická norma
Kategória: Technické normy ASTM

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Kategórie - podobné normy:

Implantáty pro chirurgii, protetiku a ortotiku
Termoplasty

Anotácia textu normy ASTM F648-14 :

Keywords:

fabricated forms, powdered form, ultra-high molecular weight polyethylene, ICS Number Code 11.040.40 (Implants for surgery, prothetics and orthotics),83.080.20 (Thermoplastic materials)

Doplňujúce informácie

1. Scope

1.1 This specification covers ultra-high molecular weight polyethylene powder (UHMWPE) and fabricated forms intended for use in surgical implants.

1.2 The requirements of this specification apply to UHMWPE in two forms. One is virgin polymer powder (Section 1.3 The requirements of this specification do not apply to UHMWPE virgin powder or fabricated forms intentionally crosslinked or blended with other additives, for example, antioxidants.

1.4 The biological response to polyethylene in soft tissue and bone has been well characterized by a history of clinical use 1.5 The values stated in SI units are to be regarded as standard.

1.6 The following precautionary caveat pertains only to the test method portion, Section 7, of this specification: 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

D1898-68(1989)	Standard Practice for Sampling of Plastics (Withdrawn 1998)
F619-20	Standard Practice for Extraction of Materials Used in Medical Devices
F748-16	Standard Practice for Selecting Generic Biological Test Methods for Materials and Devices
F749-20	Standard Practice for Evaluating Material Extracts by Intracutaneous Injection in the Rabbit
F895-11(2016)	Standard Test Method for Agar Diffusion Cell Culture Screening for Cytotoxicity
F981-23	Standard Practice for Assessment of Muscle and Bone Tissue Responses to Long-Term Implantable Materials Used in Medical Devices
D1505-18	Standard Test Method for Density of Plastics by the Density-Gradient Technique
D256-23e1	Standard Test Methods for Determining the Izod Pendulum Impact Resistance of Plastics (Includes all amendments and changes 4/7/2023).
D792-20	Standard Test Methods for Density and Specific Gravity (Relative Density) of Plastics by Displacement
D790-17	Standard Test Methods for Flexural Properties of Unreinforced and Reinforced Plastics and Electrical Insulating Materials
D648-18	Standard Test Method for Deflection Temperature of Plastics Under Flexural Load in the Edgewise Position
D638-22	Standard Test Method for Tensile Properties of Plastics
F763-22	Standard Practice for Short-Term Intramuscular Screening of Implantable Medical Device Materials
F756-17	Standard Practice for Assessment of Hemolytic Properties of Materials
F813-20	Standard Practice for Direct Contact Cell Culture Evaluation of Materials for Medical Devices
D4020-18	Standard Specification for Ultra-High-Molecular-Weight Polyethylene Molding and Extrusion Materials