Identity
- Trade Name
- Reflex 5605 EUDAMED
- Device Name
- Reflex 5605 EUDAMED
- Model / Reference
- 51005605 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 08720256103011 EUDAMED
- Basic UDI-DI
- 872025610301151005605BC EUDAMED
- EMDN Code
- Y091203 CHAIRS, TOILET AND SHOWER 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
Reflex 5605 by Lopital Nederland B.V. — 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 | 872025610301151005605BC | Class I | Active |
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Manufacturer
- Manufacturer
- Lopital Nederland B.V.
- EUDAMED SRN
- NL-MF-000004372
Sources (1)
- EUDAMED 89ef9aea-d5d7-440d-9b5e-b37cb6ce49b2 61 fields · synced Jun 18, 2026