Identity
- Trade Name
- TERUMO MEDISAFE FINETOUCH II EUDAMED
- Device Name
- Lancing Device EUDAMED
- Model / Reference
- MS*FT2R (TD-5016) EUDAMED
Identifiers
- Primary DI / UDI-DI
- 04713106024806 EUDAMED
- Basic UDI-DI
- 04698700500000PN EUDAMED
- EMDN Code
- V9099 VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- Belgium 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
Category: Device sterilization/disinfection container, reusable
Terumo Medisafe Finetouch Ii by Taidoc Technology Corporation — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS
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Also classified as Device sterilization/disinfection container, reusable.
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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 | 04698700500000PN | Class I | Active |
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Manufacturer
- Manufacturer
- TaiDoc Technology Corporation
- EUDAMED SRN
- TW-MF-000017956
- Authorised Representative
- MedNet EC-REP GmbH DE-AR-000000002
Sources (1)
- EUDAMED aa79a054-a0b4-4c49-ba28-949a0ec318a7 61 fields · synced Jun 18, 2026