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This is the free Material Data Center Datasheet of VESTAKEEP® i2 UFP10 - PEEK - Evonik Operations GmbH

Material Data Center offers the following functions for VESTAKEEP® i2 UFP10:
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Processing/Physical Characteristics - 機械的特性 - 熱的特性 - その他の特性.
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商品の説明文
Ultra-fine polyether ether ketone (PEEK) powder for permanent implants
 
VESTAKEEP® i2 UFP10 is an unreinforced, medium-viscosity, natural colored polyether ether ketone (PEEK) ultra-fine powder.

VESTAKEEP® i2 UFP10 is especially designed for long term implantable medical devices.

The semi-crystalline polymer is designed for high biocompatibility and superior mechanical, thermal and chemical resistance.

Proven Biocompatibility of VESTAKEEP® i-Grades
The biocompatibility of VESTAKEEP® i2 UFP10 has been tested following ISO 10993 recommendations for permanent tissue/bone contact. The material complies USP Class VI.

VESTAKEEP® i2 UFP10 is compliant with ASTM F2026 “Standard Specification for Polyetheretherketone (PEEK) Polymers for Surgical Implant Applications”.

A summary of biocompatibility tests is available upon request.

Biocompatibility test reports available for i2 UFP10

 
In addition to the body contact period the suitability of the material depends on further criteria, for example the nature of the contact, the processing, or the surface. In any case the suitability has to be verified for the end product.

Processing of VESTAKEEP® i-Grades
For information about processing of VESTAKEEP® i2 UFP10, please follow the general recommendations in our brochure “High Performance in Powder Form - Polyether Ether Ketone Powders“.

Delivery of VESTAKEEP® i-Grades
VESTAKEEP® i2 UFP10 is supplied as a powder in 15 kg boxes or 5 kg buckets with moisture-proof polyethylene liners.


FOR FURTHER INFORMATION PLEASE CONTACT US AT EVONIK-HP@EVONIK.COM
OR VISIT OUR PRODUCT AT  WWW.EVONIK.COM/MEDICAL-TECHNOLOGY
Processing/Physical Characteristics値単位テスト基準
ISO データ
メルトボリュームレイト, MVR 70 cm³/10min ISO 1133
温度 380 °C -
荷重 5 kg -
機械的特性値単位テスト基準
ISO データ
引張弾性率 3700 MPa ISO 527
降伏応力 100 MPa ISO 527
降伏ひずみ 5 % ISO 527
破壊呼びひずみ 30 % ISO 527
シャルピー衝撃強さ, +23°C N kJ/m² ISO 179/1eU
シャルピー衝撃強さ, -30°C N kJ/m² ISO 179/1eU
ノッチ付きシャルピー衝撃強さ, +23°C 6 kJ/m² ISO 179/1eA
Type of failure C - -
ノッチ付きシャルピー衝撃強さ, -30°C 6 kJ/m² ISO 179/1eA
Type of failure C - -
熱的特性値単位テスト基準
ISO データ
溶融温度, 10°C/min 340 °C ISO 11357-1/-3
荷重たわみ温度, 1.80 MPa 155 °C ISO 75-1/-2
荷重たわみ温度, 0.45 MPa 205 °C ISO 75-1/-2
ビカット軟化温度, B 310 °C ISO 306
その他の特性.値単位テスト基準
密度 1300 kg/m³ ISO 1183
特殊な特性
成形加工法.
コーティング., トランスファー成形.
納入形状.
パウダー., ナチュラルカラー
な特性
Thermal Stability
耐薬品性
General Chemical Resistance
Certifications
Medical Grade, Biocompatibility ISO 10993, US Pharmacopeia Class VI Approved
アプリケーション
医療の
領域別の利用可能性
北アメリカ., ヨーロッパ., アジア/太平洋地域., 南・中央アメリカ., 近東/アフリカ
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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