Identity
- Device Name
- Pep/Rmt set with mask EUDAMED
- Model / Reference
- 71103 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 07395502090035 EUDAMED
- Basic UDI-DI
- 73955026115152AN3 EUDAMED
- Direct Marketing DI
- 07395502090035 EUDAMED
- EMDN Code
- R900902 INSPIRATORY AND EXPIRATORY FLOW STIMULATORS/RESPIRATORY MUSCLES TRAINERS EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- Sweden 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
Pep/Rmt set with mask by Mediplast AB — 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 | 73955026115152AN3 | Class I | Active |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Mediplast AB
- EUDAMED SRN
- SE-MF-000000885
Sources (1)
- EUDAMED 490c6273-1016-40ef-bb6d-9bf8df9bcaf8 61 fields · synced Jul 27, 2026