Identity
- Device Name
- OriCol(TM) Sampling Device Procedure Pack EUDAMED
- Model / Reference
- PS-04 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 05060419930003 EUDAMED
- Basic UDI-DI
- 506041993PS-043V EUDAMED
- EMDN Code
- G020301 RECTAL TUBES 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
OriCol(TM) Sampling Device Procedure Pack by TOGL (Holdings) 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 | 506041993PS-043V | Class I | Active |
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Manufacturer
- Manufacturer
- TOGL (Holdings) Limited
- EUDAMED SRN
- UK-MF-000049252
- Authorised Representative
- Casus Europe B.V. NL-AR-000037688
Sources (1)
- EUDAMED 9682da3a-22af-4620-bf04-810ed4cc658e 61 fields · synced Jul 10, 2026