Identity
- Device Name
- recoveriX PRO EUDAMED
- Model / Reference
- 6451 EUDAMED6450 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 6451 EUDAMED6450 EUDAMED
- Basic UDI-DI
- ++EBCI6400LW EUDAMED
- Direct Marketing DI
- 6451 EUDAMED6450 EUDAMED
- EMDN Code
- Z120622 MUSCLE STIMULATORS EUDAMED
Classification
- Device Class
- Class IIa EUDAMED
- Market of Registration
- Austria 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
Yes
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
recoveriX PRO by g.tec medical engineering GmbH — Class IIa — 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 | ++EBCI6400LW | Class IIa | Active |
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Manufacturer
- Manufacturer
- g.tec medical engineering GmbH
- EUDAMED SRN
- AT-MF-000004562
Sources (2)
- EUDAMED 4b5d20f7-8bc3-4e71-98e3-8d43452f5992 61 fields · synced Jul 29, 2026
- EUDAMED 6ae19fb9-8612-4d72-bff1-40df05f9f325 61 fields · synced May 19, 2026