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外科植入物用聚L-丙交酯树脂及制品检测

发布时间:2024-05-27 17:49:26 - 更新时间:2024年06月29日 15:22

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军工检测 其他检测

YY/T 0474-2004 L-.体降解试验

本标准描述了聚L-丙交酯在体外降解试验条件下化学或机械性能变化的测定方法。 本标准的目的在于比较和(或)评价材料或加工条件。 本标准适用于生产外科植入物的各种形态的聚L丙交酯。包括: a)块材; b)加工材; c)最终产品(经包装和灭菌的植入物

Poly(L-lactide) resins and fabricated forms for surgical implants-In vitro degradation testing

ISO 13781:1997 L-.体降解试验

Describes methods for the determination of chemical and mechanical changes in properties of poly(L-lactide) under in vitro degradation testing

Poly(L-lactide) resins and fabricated forms for surgical implants - In vitro degradation testing

YY/T 0510-2009 定形-乙

本标准适用于能在30℃被二氯甲烷或三氯甲烷完全溶解的原生聚丙交酯和丙交酯-乙交酯共聚树脂。本标准所述的聚D,L-丙交酯均聚物是指定形的(即结晶性)、由内消旋丙交酯或等摩尔的D丙交酯和L-丙交酯(外消旋)聚合而成。本标准所述的D,L丙交酯-乙交酯共聚物也是指定形的、 由乙交酯和内消旋丙交酯或等

Amorphous Poly(lactide) and Poly(lactide-co-glyclide) Resins for Surgical Implants

KS P ISO 13781:2008 L.造形状.体分解试验

이 표준은 체외에서의 분해 시험 상태에서 일어나는 폴리(L-락티드)의 화학적 및 기계적 특

Poly(L-lactide) resins and fabricated forms for surgical implants-In vitro degradation testing

YY/T 0661-2017 半结晶型和共

本标准适用于外科植入物用聚(L-乳酸)树脂(或缩写PLLA树脂)。但不包括D,L型立体异构体或任何比率的DL型共聚体。 本标准阐述了聚(L-乳酸)树脂的性能,不适用于此材料加工的经过包装、灭菌的成品植入物。 本标准采用国际单位制(SI)。 本标准并非试图对所涉及的所有安全问题进行阐述,即便是与

Standard specification for virgin poly(L-lactic acid) resin for surgical implants

GOST R ISO 13781-2011 (L-)作形式.体老化试验

Poly(L-lactide) resins and fabricated forms for surgical implants. In vitro degradation testing

ASTM F2579-06 定型的的标准规范

1.1 This specification covers virgin poly(lactide) and poly(lactide-co-glycolide) resins able to be fully solvated at 30176;C by either methylene

Standard Specification for Amorphous Poly(lactide) and Poly(lactide-co-glycolide) Resins for Surgical Implants

ASTM F2579-06e1 定型的的标准规范

1.1 This specification covers virgin poly(lactide) and poly(lactide-co-glycolide) resins able to be fully solvated at 30176;C by either methylene

Standard Specification for Amorphous Poly(lactide) and Poly(lactide-co-glycolide) Resins for Surgical Implants

ASTM F2579-08 定型的的标准规范

1.1 This specification covers virgin poly(lactide) and poly(lactide-co-glycolide) resins able to be fully solvated at 30

Standard Specification for Amorphous Poly(lactide) and Poly(lactide-co-glycolide) Resins for Surgical Implants

ASTM F1925-22 半结晶和共的标准规范

Standard Specification for Semi-Crystalline Poly(lactide) Polymer and Copolymer Resins for Surgical Implants

ASTM F1925-17 的半结晶和共的标准规范

Standard Specification for Semi-Crystalline Poly(lactide) Polymer and Copolymer Resins for Surgical Implants

DB31/ 183-1996 --烯酸骨水泥

YY/T 0661-2008 L-乳酸)的标准规范

本标准适用于外科植入物用聚(L-乳酸)树脂(或缩写PLLA树脂)。但不包括D,L型立体异构体或任何比率的DL型共聚体。 本标准阐述了聚(L-乳酸)树脂的性能,不适用于此材料加工的经过包装、灭菌的成品植入物。 本标准采用国际单位制(SI)。 本标准并非试图对所涉及的所有安全问题进行阐述,即便是与

Standard specification for virgin poly(L-lactic acid) resin for surgical implants

NF S90-430:1979 .接骨粘合剂

MEDICAL AND SURGICAL EQUIPMENT. IMPLANTS FOR SURGERY. ACRYLIC RESIN BONE CEMENTS.

AS 5833-2005 烯酸水泥

Adopts ISO 5833:2002, to specify the physical, mechanical, packaging and labelling requirements for curing polymerizing radio-opaque

Implants for surgery - Acrylic resin cements

YY/T 0474-2004 L-.体降解试验

本标准描述了聚L-丙交酯在体外降解试验条件下化学或机械性能变化的测定方法。 本标准的目的在于比较和(或)评价材料或加工条件。 本标准适用于生产外科植入物的各种形态的聚L丙交酯。包括: a)块材; b)加工材; c)最终产品(经包装和灭菌的植入物

Poly(L-lactide) resins and fabricated forms for surgical implants-In vitro degradation testing

ISO 13781:1997 L-.体降解试验

Describes methods for the determination of chemical and mechanical changes in properties of poly(L-lactide) under in vitro degradation testing

Poly(L-lactide) resins and fabricated forms for surgical implants - In vitro degradation testing

YY/T 0510-2009 定形-乙

本标准适用于能在30℃被二氯甲烷或三氯甲烷完全溶解的原生聚丙交酯和丙交酯-乙交酯共聚树脂。本标准所述的聚D,L-丙交酯均聚物是指定形的(即结晶性)、由内消旋丙交酯或等摩尔的D丙交酯和L-丙交酯(外消旋)聚合而成。本标准所述的D,L丙交酯-乙交酯共聚物也是指定形的、 由乙交酯和内消旋丙交酯或等

Amorphous Poly(lactide) and Poly(lactide-co-glyclide) Resins for Surgical Implants

KS P ISO 13781:2008 L.造形状.体分解试验

이 표준은 체외에서의 분해 시험 상태에서 일어나는 폴리(L-락티드)의 화학적 및 기계적 특

Poly(L-lactide) resins and fabricated forms for surgical implants-In vitro degradation testing

YY/T 0661-2017 半结晶型和共

本标准适用于外科植入物用聚(L-乳酸)树脂(或缩写PLLA树脂)。但不包括D,L型立体异构体或任何比率的DL型共聚体。 本标准阐述了聚(L-乳酸)树脂的性能,不适用于此材料加工的经过包装、灭菌的成品植入物。 本标准采用国际单位制(SI)。 本标准并非试图对所涉及的所有安全问题进行阐述,即便是与

Standard specification for virgin poly(L-lactic acid) resin for surgical implants

GOST R ISO 13781-2011 (L-)作形式.体老化试验

Poly(L-lactide) resins and fabricated forms for surgical implants. In vitro degradation testing

ASTM F2579-06 定型的的标准规范

1.1 This specification covers virgin poly(lactide) and poly(lactide-co-glycolide) resins able to be fully solvated at 30176;C by either methylene

Standard Specification for Amorphous Poly(lactide) and Poly(lactide-co-glycolide) Resins for Surgical Implants

ASTM F2579-06e1 定型的的标准规范

1.1 This specification covers virgin poly(lactide) and poly(lactide-co-glycolide) resins able to be fully solvated at 30176;C by either methylene

Standard Specification for Amorphous Poly(lactide) and Poly(lactide-co-glycolide) Resins for Surgical Implants

ASTM F2579-08 定型的的标准规范

1.1 This specification covers virgin poly(lactide) and poly(lactide-co-glycolide) resins able to be fully solvated at 30

Standard Specification for Amorphous Poly(lactide) and Poly(lactide-co-glycolide) Resins for Surgical Implants

ASTM F1925-22 半结晶和共的标准规范

Standard Specification for Semi-Crystalline Poly(lactide) Polymer and Copolymer Resins for Surgical Implants

ASTM F1925-17 的半结晶和共的标准规范

Standard Specification for Semi-Crystalline Poly(lactide) Polymer and Copolymer Resins for Surgical Implants

DB31/ 183-1996 --烯酸骨水泥

YY/T 0661-2008 L-乳酸)的标准规范

本标准适用于外科植入物用聚(L-乳酸)树脂(或缩写PLLA树脂)。但不包括D,L型立体异构体或任何比率的DL型共聚体。 本标准阐述了聚(L-乳酸)树脂的性能,不适用于此材料加工的经过包装、灭菌的成品植入物。 本标准采用国际单位制(SI)。 本标准并非试图对所涉及的所有安全问题进行阐述,即便是与

Standard specification for virgin poly(L-lactic acid) resin for surgical implants

NF S90-430:1979 .接骨粘合剂

MEDICAL AND SURGICAL EQUIPMENT. IMPLANTS FOR SURGERY. ACRYLIC RESIN BONE CEMENTS.

AS 5833-2005 烯酸水泥

Adopts ISO 5833:2002, to specify the physical, mechanical, packaging and labelling requirements for curing polymerizing radio-opaque

Implants for surgery - Acrylic resin cements

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