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3M™ Viscoplast™ active plastry piankowe
EUDAMEDClass I (EU MDR)
Ref N17020100Model V9-8-2
Identity
- Device Name
- 3M™ Viscoplast™ active plastry piankowe EUDAMED
- Model / Reference
- V9-8-2 EUDAMEDN17020100 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 04054596758223 EUDAMED
- Basic UDI-DI
- 06082232761050000000009GR EUDAMED
- EMDN Code
- M04010102 POLYURETHANE (OR OTHER MATERIAL) ADHESIVE DRESSINGS, WITH ABSORBENT PAD 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
3M™ Viscoplast™ active plastry piankowe by 3M Deutschland GmbH (Medical) — 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 | 06082232761050000000009GR | Class I | Active |
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Manufacturer
- Manufacturer
- 3M Deutschland GmbH (Medical)
- EUDAMED SRN
- DE-MF-000011641
Sources (1)
- EUDAMED bcd790eb-27be-41ec-a55c-4fa1f9dd612c 61 fields · synced Jun 19, 2026