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Remove Orientation Device Ø22
EUDAMEDClass I (EU MDR)
Ref HQA VI004Model Class I Instrument
Identity
- Trade Name
- REMOVE ORIENTATION DEVICE Ø22 EUDAMED
- Device Name
- Class I Instrument EUDAMED
- Model / Reference
- Class I Instrument EUDAMEDHQA VI004 EUDAMED
Identifiers
- Primary DI / UDI-DI
- +M483HQAVI0040 EUDAMED
- Basic UDI-DI
- ++M483L0999ZW EUDAMED
- Direct Marketing DI
- +M483HQAVI0040 EUDAMED
- EMDN Code
- L0999 ORTHOPAEDIC AND TRAUMATOLOGICAL SURGERY INSTRUMENTS, REUSABLE - OTHER EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- France 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
Remove Orientation Device Ø22 by groupe lépine — 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 | ++M483L0999ZW | Class I | Active |
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Manufacturer
- Manufacturer
- groupe lépine
- EUDAMED SRN
- FR-MF-000001182
Sources (1)
- EUDAMED 6f487b39-6e5f-4d97-ae06-93c6b26d191a 61 fields · synced Jun 19, 2026