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Danafast Tubular retention bandage
EUDAMEDClass I (EU MDR)
Ref 6050772
by Mediplast AB
Identity
- Device Name
- Danafast Tubular retention bandage EUDAMEDDanafast Tubular retention bandage, viscose EUDAMED
- Model / Reference
- 6050772 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 07395502097058 EUDAMED
- Basic UDI-DI
- 73955026107115AMZ EUDAMED
- Direct Marketing DI
- 07395502097058 EUDAMED
- EMDN Code
- M03030201 TUBULAR MESH 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
Danafast Tubular retention bandage 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 | 73955026107115AMZ | Class I | Active |
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Manufacturer
- Manufacturer
- Mediplast AB
- EUDAMED SRN
- SE-MF-000000885
Sources (2)
- EUDAMED 92b6bfaa-a860-41dd-90e7-943ebc676f5e 61 fields · synced Jun 20, 2026
- EUDAMED ed2f8492-46b9-4fa2-b5d7-f98b84322bb4 61 fields · synced Jun 20, 2026