Identity
- Trade Name
- resi OPEP EUDAMED
- Device Name
- resi opep respiratory therapy device EUDAMED
- Model / Reference
- resi1 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 07640372030170 EUDAMED
- Basic UDI-DI
- 764037203resi1ZT EUDAMED
- Direct Marketing DI
- 07640372030170 EUDAMED
- EMDN Code
- R900902 INSPIRATORY AND EXPIRATORY FLOW STIMULATORS/RESPIRATORY MUSCLES TRAINERS EUDAMED
Classification
- Device Class
- Class I 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
resi OPEP by Anel 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 | 764037203resi1ZT | Class I | Active |
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Manufacturer
- Manufacturer
- Anel AG
- EUDAMED SRN
- CH-MF-000033240
- Authorised Representative
- International Associates Auditing & Certification Limited IE-AR-000002248
Sources (1)
- EUDAMED fb4dd705-e7d1-428b-99ae-d5c907f7421f 61 fields · synced Jul 18, 2026