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catalyst paste futur 23 ml Puresil
EUDAMEDClass IIa (EU MDR)
Ref 03713 / ACC136
Identity
- Trade Name
- catalyst paste futur 23 ml Puresil EUDAMED
- Device Name
- Ohr-Abdruckmaterial, Silikongummi EUDAMED
- Model / Reference
- 03713 / ACC136 EUDAMED
Identifiers
- Primary DI / UDI-DI
- +EDET037131 EUDAMED
- Basic UDI-DI
- ++EDET0185R EUDAMED
- EMDN Code
- Q030499 OTOLOGY DEVICES - OTHER EUDAMED
Classification
- Device Class
- Class IIa EUDAMED
- Market of Registration
- Northern Ireland EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Implantable
No
EUDAMED
Reusable
No
EUDAMED
Contains Latex
No
EUDAMED
Reprocessed
No
EUDAMED
CMR Substance
Yes
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
catalyst paste futur 23 ml Puresil by DETAX GmbH & Co. KG — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union No Longer Active
CE/MDR
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | ++EDET0185R | Class IIa | No Longer Active |
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Manufacturer
- Manufacturer
- DETAX GmbH & Co. KG
- EUDAMED SRN
- DE-MF-000005995
Sources (1)
- EUDAMED 300bfd2d-1bac-4a20-bb50-91cae0c2f9dc 61 fields · synced Jun 19, 2026