Integra® Dermal Regeneration Template
by Integra LifeSciences Corporation 14 variants
Ref 64101T
Active
CE MDD
Valid until
Not listed
FDA recalls
Not applicable
Documents
None linked in EUDAMED
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDD | NumberB-10381780356264 10381780356264 | Date10 Sep 2026 | StatusActive |
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDD Active
Specification
- Device Name
- Integra Meshed Dermal Regeneration Template, Integra Dermal Regeneration Template - Terminally Sterilized, Single Layer, Thin
- Model / Reference
- 64101T
- Primary DI / UDI-DI
- 10381780356264
- Basic UDI-DI
- B-10381780356264
- EMDN Code
- P900402 Resorbable filling and reconstruction devices
- Device Class
- Class III
- EU market of registration
- Belgium
Manufacturer details
- EUDAMED SRN
- US-MF-000007196
- Authorised representative
- Integra LifeSciences Services FR-AR-000002474
Other devices from Integra Lifesciences Corp.
Properties
Other properties (10)
- Reusable: No
- Contains Latex: No
- Reprocessed: No
- CMR Substance: No
- Human-derived: No
- Human Tissues: No
- Endocrine Disruptor: No
- Administering Medicine: No
- Measuring Function: No
- Incorporates Medicinal Product: No