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This is the free Material Data Center Datasheet of VESTAKEEP® Care M20 G - PEEK - Evonik Operations GmbH

Material Data Center offers the following functions for VESTAKEEP® Care M20 G:
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제품 설명서
Medium viscosity, unreinforced polyether ether ketone designed for the medical device industry

VESTAKEEP® Care is the ideal materials for the fabrication of medical devices with short time contact to human blood, tissue or bone for up to 30 days. VESTAKEEP® Care Grades have a good biocompatibility, processability and the option to pigment.

VESTAKEEP® Care M20 G is a medium viscosity, unreinforced polyether ether ketone for injection molding.

The semi-crystalline polymer features superior thermal and chemical resistance.

Biocompatibility of VESTAKEEP® Care
In an extensive testing program run by independent certified labs, biocompatibility has been tested following United States Pharmacopeia and ISO 10933-1:2003 guidelines.
The test reports attest VESTAKEEP® Care’s excellent biocompatibility.

Biocompatibility tests for VESTAKEEP® Care:

 
Processing of VESTAKEEP® Care
VESTAKEEP® Care resins can be processed using all conventional melt processing techniques such as injection moulding, extrusion, and compression moulding.

VESTAKEEP® Care M20 G can be processed by common machines for thermoplastics. We recommend a melt temperature between 360°C and 380°C during the injection molding process. The mold temperature should be within a range of 160°C to 200°C, preferably 180°C.

Our technical experts would appreciate to give you support regarding the special requirements for the processing of VESTAKEEP® Care M20 G.

Delivery of VESTAKEEP® Care
VESTAKEEP® Care M20 G is supplied as granules in 25 kg boxes with moisture-proof polyethylene liners.


The results shown have been generated from a low number of production lots. Therefore, they are preliminary and not yet the result of a statistical evaluation. Therefore they must not be used to establish specifications.

FOR FURTHER INFORMATION PLEASE CONTACT US AT EVONIK-HP@EVONIK.COM
OR VISIT OUR PRODUCT AT  WWW.EVONIK.COM/MEDICAL-TECHNOLOGY 


 
Processing/Physical Characteristics단위시험규격
ISO 데이터
용융 부피 - 흐름 속도, MVR 70 cm³/10min ISO 1133
온도 380 °C -
하중 5 kg -
성형 수축률, 평행 1.1 % ISO 294-4, 2577
성형 수축률, 수직 1.1 % ISO 294-4, 2577
기계적 특성단위시험규격
ISO 데이터
인장탄성률 3700 MPa ISO 527
항복강도 100 MPa ISO 527
항복변형률 5 % ISO 527
파단시 평균신율 40 % ISO 527
챠피 충격 강도 , +23°C N kJ/m² ISO 179/1eU
챠피 충격 강도, -30°C N kJ/m² ISO 179/1eU
챠피 노치드 충격 강도, +23°C 6 kJ/m² ISO 179/1eA
Type of failure C - -
챠피 노치드 충격 강도, -30°C 6 kJ/m² ISO 179/1eA
Type of failure C - -
열적 특성단위시험규격
ISO 데이터
비카트 연화 온도, B 310 °C ISO 306
선형 열팽창 계수, 평행 60 E-6/K ISO 11359-1/-2
전기적 특성단위시험규격
ISO 데이터
상대 유전뮬, 1MHz 2.8 - IEC 62631-2-1
부피 저항 >1E13 Ohm*m IEC 62631-3-1
CTI 200 - IEC 60112
기타 특성단위시험규격
밀도 1300 kg/m³ ISO 1183
특징
생산 공정
사출 성형
인도 유형
펠렛 (입자,알갱이)
특성
Thermal Stability
내화학성에
General Chemical Resistance
Certifications
Medical Grade, Biocompatibility ISO 10993, US Pharmacopeia Class VI Approved
응용
의료
지역별 검색
쨘횕쩐횈쨍횧쨍짰횆짬, 짱쨌쨈, 쩐횈쩍횄쩐횈 횇횂횈챵쩐챌 횁철쩔짧, 쨀짼쨘횓 쨔횞 횁횩쩐횙 쩐횈쨍횧쨍짰횆짬, 쨉쩔쩐챌 쨔횞 쩐횈횉횁쨍짰횆짬 짹횢쩔짧
Disclaimer
Copyright Altair Engineering GmbH. Altair Engineering GmbH assumes no liability for the system to be free of errors. The user takes sole responsibility for the use of this data under the exclusion of every liability from Altair Engineering GmbH; this is especially valid for claims of compensation resulting from consequential damages. Altair explicitly points out that any decision about the application of materials must be double checked with the producer of this material. This includes all contents of this system. Copyright laws are applicable for the content of this system.
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