Identity
- Trade Name
- Extrem Wasserfest Pflaster EUDAMED
- Device Name
- Pflaster EUDAMED
- Model / Reference
- 03-009 EUDAMED02-045 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 04260206626763 EUDAMED04260206622031 EUDAMED
- Basic UDI-DI
- 426020662apf1F5 EUDAMED
- Direct Marketing DI
- 04260206626763 EUDAMED04260206622031 EUDAMED
- EMDN Code
- M0599 MEDICAL PLASTERS - OTHER 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
Extrem Wasserfest Pflaster by WUNDmed GmbH & Co. KG — 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 | 426020662apf1F5 | Class I | Active |
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Manufacturer
- Manufacturer
- WUNDmed GmbH & Co. KG
- EUDAMED SRN
- DE-MF-000010322
Sources (2)
- EUDAMED c396e560-8d6b-4f67-bfda-f1a1efb10877 61 fields · synced Oct 5, 2026
- EUDAMED 6aafa85c-0a84-4350-a8a7-d7fae7330703 61 fields · synced May 18, 2026