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Danafast Tubular retention bandage
EUDAMEDClass I (EU MDR)
Ref 6050775
by Mediplast AB
Identity
- Device Name
- Danafast Tubular retention bandage EUDAMED
- Model / Reference
- 6050775 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 07395502097089 EUDAMED
- Basic UDI-DI
- 73955026107115AMZ EUDAMED
- Direct Marketing DI
- 07395502097089 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 (1)
- EUDAMED 4c847237-a093-4c2a-ae20-a53d4c302071 61 fields · synced Jun 18, 2026