Identity
- Trade Name
- RheoConnect 1.0 Philips EUDAMEDRheoConnect 1.0 Philips Longer EUDAMED
- Device Name
- RheoConnect 1.0 EUDAMED
- Model / Reference
- 22010 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 07649989882028 EUDAMED07649989882134 EUDAMED
- Basic UDI-DI
- 7649989882RCN1.02N EUDAMED
- Direct Marketing DI
- 07649989882028 EUDAMED07649989882134 EUDAMED
- EMDN Code
- Z12109006 BRAIN TISSUE MONITORING SYSTEMS EUDAMED
Classification
- Device Class
- Class I 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
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
RheoConnect 1.0 Philips by Luciole Medical AG — 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 | 7649989882RCN1.02N | Class I | Active |
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Manufacturer
- Manufacturer
- Luciole Medical AG
- EUDAMED SRN
- CH-MF-000015856
- Authorised Representative
- Veranex Germany GmbH DE-AR-000005578
Sources (2)
- EUDAMED e81d5a34-9e08-4bf1-bbd6-e25f02b70fc0 61 fields · synced Jul 30, 2026
- EUDAMED bc78821e-78b1-47cb-82fd-b571c54e836c 61 fields · synced May 18, 2026