Identity
- Trade Name
- M9 Trauma EUDAMED
- Device Name
- M9 Stretcher EUDAMED
- Model / Reference
- M9 Trauma Stretcher EUDAMEDM93244+11+131 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 09344090011944 EUDAMED
- Basic UDI-DI
- 942904017343M9Stretcher3J EUDAMED
- EMDN Code
- V08050101 GENERIC USE STRETCHERS EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- Netherlands EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Implantable
No
EUDAMED
Reusable
No
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
M9 Trauma by Howard Wright Limited — 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 | 942904017343M9Stretcher3J | Class I | Active |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Howard Wright Limited
- EUDAMED SRN
- NZ-MF-000009802
- Authorised Representative
- Advena Limited MT-AR-000000234
Sources (1)
- EUDAMED 0efa45a8-42d0-4eef-84fe-55eb8ea8402b 61 fields · synced Jun 17, 2026