Identity
- Trade Name
- AIVIA EUDAMED
- Device Name
- Aivia V3 Protection model 200 EUDAMED
- Model / Reference
- X3A200-XX101 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 03770023276023 EUDAMED
- Basic UDI-DI
- 37700AIVIA-V3-2005A EUDAMED
- Direct Marketing DI
- 03770023276023 EUDAMED
- EMDN Code
- C020480 CARDIOVERSION AND EXTERNAL DEFIBRILLATION DEVICES - ACCESSORIES EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- France 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
Aivia by Pyrescom — 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 | 37700AIVIA-V3-2005A | Class I | Active |
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Manufacturer
- Manufacturer
- Pyrescom
- EUDAMED SRN
- FR-MF-000007671
Sources (1)
- EUDAMED 215f5093-89a4-4738-9c04-e2f4871e0c67 61 fields · synced Jun 19, 2026