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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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
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
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
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
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
Poly(L-lactide) resins and fabricated forms for surgical implants. In vitro degradation testing
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
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
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 Standard Specification for Semi-Crystalline Poly(lactide) Polymer and Copolymer Resins for Surgical Implants Standard Specification for Semi-Crystalline Poly(lactide) Polymer and Copolymer Resins for Surgical Implants 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 MEDICAL AND SURGICAL EQUIPMENT. IMPLANTS FOR SURGERY. ACRYLIC RESIN BONE CEMENTS. Adopts ISO 5833:2002, to specify the physical, mechanical, packaging and labelling requirements for curing polymerizing radio-opaque Implants for surgery - Acrylic resin cements 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 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 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 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 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 Poly(L-lactide) resins and fabricated forms for surgical implants. In vitro degradation testing 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 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 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 Standard Specification for Semi-Crystalline Poly(lactide) Polymer and Copolymer Resins for Surgical Implants Standard Specification for Semi-Crystalline Poly(lactide) Polymer and Copolymer Resins for Surgical Implants 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 MEDICAL AND SURGICAL EQUIPMENT. IMPLANTS FOR SURGERY. ACRYLIC RESIN BONE CEMENTS. Adopts ISO 5833:2002, to specify the physical, mechanical, packaging and labelling requirements for curing polymerizing radio-opaque Implants for surgery - Acrylic resin cements ASTM F1925-22 外科植入物用半结晶聚丙交酯聚合物和共聚物树脂的标准规范
ASTM F1925-17 用于外科植入物的半结晶聚(丙交酯)聚合物和共聚物树脂的标准规范
DB31/ 183-1996 外科植入物--丙烯酸酯类树脂骨水泥
YY/T 0661-2008 外科植入物用聚(L-乳酸)树脂的标准规范
NF S90-430:1979 外科植入物.聚丙烯树脂接骨粘合剂
AS 5833-2005 外科用植入物.丙烯酸树脂水泥
YY/T 0474-2004 外科植入物用聚L-丙交酯树脂及制品.体外降解试验
ISO 13781:1997 外科植入物用聚L-交酯树脂及制品.体外降解试验
YY/T 0510-2009 外科植入物用定形聚丙交酯树脂和丙交酯-乙交酯共聚树脂
KS P ISO 13781:2008 外科值入物用聚L.丙交酯树脂及其制造形状.体外分解试验
YY/T 0661-2017 外科植入物 半结晶型聚丙交酯聚合物和共聚物树脂
GOST R ISO 13781-2011 外科植入物用聚(L-交酯)树脂和制作形式.体外老化试验
ASTM F2579-06 外科植入物用定型的聚丙交酯和丙交酯乙交酯共聚物树脂的标准规范
ASTM F2579-06e1 外科植入物用定型的聚丙交酯和丙交酯乙交酯共聚物树脂的标准规范
ASTM F2579-08 外科植入物用定型的聚丙交酯和丙交酯乙交酯共聚物树脂的标准规范
ASTM F1925-22 外科植入物用半结晶聚丙交酯聚合物和共聚物树脂的标准规范
ASTM F1925-17 用于外科植入物的半结晶聚(丙交酯)聚合物和共聚物树脂的标准规范
DB31/ 183-1996 外科植入物--丙烯酸酯类树脂骨水泥
YY/T 0661-2008 外科植入物用聚(L-乳酸)树脂的标准规范
NF S90-430:1979 外科植入物.聚丙烯树脂接骨粘合剂
AS 5833-2005 外科用植入物.丙烯酸树脂水泥