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Revitive Circulation Booster
EUDAMEDClass IIa (EU MDR)
Ref 5572AQModel 5572AQ-FR-BEN
Identity
- Trade Name
- Revitive Circulation Booster EUDAMED
- Device Name
- Revitive ProHealth EUDAMED
- Model / Reference
- 5572AQ-FR-BEN EUDAMED5572AQ EUDAMED
Identifiers
- Primary DI / UDI-DI
- 05060217496404 EUDAMED
- Basic UDI-DI
- B-05060217496404 EUDAMED
- EMDN Code
- Z120622 MUSCLE STIMULATORS EUDAMED
Classification
- Device Class
- Class IIa EUDAMED
- Market of Registration
- France EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Implantable
No
EUDAMED
Reusable
No
EUDAMED
Contains Latex
No
EUDAMED
Reprocessed
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Revitive Circulation Booster by Actegy Limited — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/MDD
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | B-05060217496404 | Class IIa | Active |
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Manufacturer
- Manufacturer
- Actegy Limited
- EUDAMED SRN
- GB-MF-000032543
- Authorised Representative
- MDSS GmbH DE-AR-000005430
Sources (1)
- EUDAMED 7bc36771-2264-4b8e-ac44-b41b3603b6ad 61 fields · synced Jun 19, 2026