← Back to catalogue
Ristocetin (7.5 mg/vial)
EUDAMEDClass IVD General (EU MDR)
Ref 50705Model Ristocetin (7.5 mg/vial)
Identity
- Trade Name
- Ristocetin (7.5 mg/vial) EUDAMED
- Device Name
- Ristocetin (7.5 mg/vial) EUDAMED
- Model / Reference
- Ristocetin (7.5 mg/vial) EUDAMED50705 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 05391521420084 EUDAMED
- Basic UDI-DI
- B-05391521420084 EUDAMED
- EMDN Code
- W0103020401 AGGREGATION REAGENTS EUDAMED
Classification
- Device Class
- Class IVD General EUDAMED
- Market of Registration
- Austria EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Microbial Substances
No
EUDAMED
Reagent
Yes
EUDAMED
Self Testing
No
EUDAMED
Near-Patient Testing
No
EUDAMED
Professional Testing
Yes
EUDAMED
Companion Diagnostics
No
EUDAMED
Surgical Instrument
No
EUDAMED
Ristocetin (7.5 mg/vial) by Tcoag ireland ltd — Class IVD General — IVDD — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/IVDD
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/IVDD | B-05391521420084 | Class IVD General | Active |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Tcoag ireland ltd
- EUDAMED SRN
- IE-MF-000027371
Sources (1)
- EUDAMED d4a0b253-8696-494e-95a6-e7b24e10d75c 61 fields · synced Jun 18, 2026