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Emergency control Anteris 30
EUDAMEDClass I (EU MDR)
Ref 101.0762.0Model Anteris
Identity
- Trade Name
- Emergency control Anteris 30 EUDAMED
- Device Name
- Anteris - operating table EUDAMED
- Model / Reference
- Anteris EUDAMED101.0762.0 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 04049199011516 EUDAMED
- Basic UDI-DI
- 4049199ANTERIS2E EUDAMED
- EMDN Code
- Z12011202,Z12011280 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
Emergency control Anteris 30 by SCHMITZ medical 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 | 4049199ANTERIS2E | Class I | Active |
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Manufacturer
- Manufacturer
- SCHMITZ medical GmbH
- EUDAMED SRN
- DE-MF-000008189
Sources (1)
- EUDAMED ba33a0c0-605a-48e7-ba8e-526f0c39e77b 61 fields · synced Jul 15, 2026