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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:
unit conversion, PDF datasheet print, comparison with other plastics, snap fit calculation, beam deflection calculation, CAE Interfaces
unit conversion, PDF datasheet print, comparison with other plastics, snap fit calculation, beam deflection calculation, CAE Interfaces
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Informations produit
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
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.
The values presented are typical or average values, they do not constitute a specification.
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
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.
The values presented are typical or average values, they do not constitute a specification.
FOR FURTHER INFORMATION PLEASE CONTACT US AT EVONIK-HP@EVONIK.COM
OR VISIT OUR PRODUCT AT WWW.EVONIK.COM/MEDICAL-TECHNOLOGY
| Caractéristiques des transformations/physiques | Valeur | Unité | Norme du test | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| ISO Data | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Indice de fluidité à chaud en volume, MVR | 70 | cm³/10min | ISO 1133 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Température | 380 | °C | - | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Charge | 5 | kg | - | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Propriétés mécaniques | Valeur | Unité | Norme du test | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| ISO Data | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Module en traction | 3700 | MPa | ISO 527 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Contrainte d'écoulement | 100 | MPa | ISO 527 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Déformation au seuil d'écoulement | 5 | % | ISO 527 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Déformation nominale à la rupture | 30 | % | ISO 527 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Résistance au choc Charpy, +23°C | N | kJ/m² | ISO 179/1eU | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Résistance au choc Charpy, -30°C | N | kJ/m² | ISO 179/1eU | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Résistance au choc Charpy (entaillé), +23°C | 6 | kJ/m² | ISO 179/1eA | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Type de défaillance | C | - | - | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Résistance au choc Charpy (entaillé), -30°C | 6 | kJ/m² | ISO 179/1eA | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Type de défaillance | C | - | - | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Propriétés thermiques | Valeur | Unité | Norme du test | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| ISO Data | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Température de fusion, 10°C/min | 340 | °C | ISO 11357-1/-3 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Température de fléchissement s/chrg, 1.80 MPa | 155 | °C | ISO 75-1/-2 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Température de fléchissement s/chrg, 0.45 MPa | 205 | °C | ISO 75-1/-2 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Température de ramolliss. Vicat, B | 310 | °C | ISO 306 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Propriétés diverses | Valeur | Unité | Norme du test |
| Masse volumique | 1300 | kg/m³ | ISO 1183 |
Caractéristiques
Transformation
Enduction, Moulage par transfert
Conditionnement
Poudre, Couleurs naturelles
Caractéristiques
Stabilité thermique
Résistance Chimique
Résistance chimique générale
Certifications
Grade médical, Biocompatibility ISO 10993, USP Class VI approbation
Applications
Médical
Disponibilité régionale
Amérique du nord, Europe, Asia Pacific, South and Central America, Proche-Orient/Afrique
Conditions générales
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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