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Prodisc-L Poly Inlay Remover
EUDAMEDClass I (EU MDR)
Ref 03.820.201Model Reusable instrumentation
Identity
- Trade Name
- PRODISC-L POLY INLAY REMOVER EUDAMED
- Model / Reference
- Reusable instrumentation EUDAMED03.820.201 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 00843193117793 EUDAMED
- Basic UDI-DI
- 08431931InstrumentsU5 EUDAMED
- EMDN Code
- L091101 ORTHOPAEDIC PROSTHESES AND TRAUMATOLOGICAL IMPLANTS EXTRACTORS, REUSABLE EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- Germany EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Implantable
No
EUDAMED
Reusable
Yes
EUDAMED
Contains Latex
No
EUDAMED
Reprocessed
No
EUDAMED
CMR Substance
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Prodisc-L Poly Inlay Remover by Centinel Spine, LLC — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/MDR
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 08431931InstrumentsU5 | Class I | Active |
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Manufacturer
- Manufacturer
- Centinel Spine, LLC
- EUDAMED SRN
- US-MF-000013245
- Authorised Representative
- Emergo Europe B.V. NL-AR-000000116
Sources (1)
- EUDAMED d0231ab1-bdff-4573-ab3d-fa11d894e3b8 61 fields · synced Jul 31, 2026