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ORBIS Adhaesiv-Liquid
EUDAMEDClass I (EU MDR)
Ref 193079Model 122
by PRISMAN GmbH
Identity
- Trade Name
- ORBIS Adhaesiv-Liquid EUDAMED
- Device Name
- Adhäsiv Liquid SILICON EUDAMED
- Model / Reference
- 122 EUDAMED193079 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 04064797030387 EUDAMED
- Basic UDI-DI
- ++EPRM122DF EUDAMED
- EMDN Code
- Q01020104 DENTAL IMPRESSION SILICONES EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- Germany 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
ORBIS Adhaesiv-Liquid by PRISMAN GmbH — 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 | ++EPRM122DF | Class I | Active |
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Manufacturer
- Manufacturer
- PRISMAN GmbH
- EUDAMED SRN
- DE-MF-000009900
Sources (1)
- EUDAMED 1b2a76e8-af90-4519-be3e-47bc086da953 61 fields · synced Jul 16, 2026