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Ventilution
EUDAMEDClass IIa (EU MDR)
Ref 000070Model Ventilution Patient Set Standard
Identity
- Trade Name
- Ventilution EUDAMED
- Device Name
- Ventilution Patient Set Standard EUDAMED
- Model / Reference
- Ventilution Patient Set Standard EUDAMED000070 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 04262371370014 EUDAMED
- Basic UDI-DI
- 426237137000952BS EUDAMED
- Direct Marketing DI
- 04262371370014 EUDAMED
- EMDN Code
- R9099 RESPIRATORY AND ANAESTHESIA DEVICES - OTHER EUDAMED
Classification
- Device Class
- Class IIa 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
Category: Pulmonary function analysis system, adult
Ventilution by Gründler GmbH — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS
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Also classified as Pulmonary function analysis system, adult.
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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 | 426237137000952BS | Class IIa | Active |
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Manufacturer
- Manufacturer
- Gründler GmbH
- EUDAMED SRN
- DE-MF-000025923
Sources (1)
- EUDAMED 180d23ba-de2c-455f-a7d7-b7f85476b77d 61 fields · synced Jun 19, 2026