Identity
- Trade Name
- Ichthopaste EUDAMED
- Device Name
- Ichthopaste EUDAMED
- Model / Reference
- 4959 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 07350041580966 EUDAMED
- Basic UDI-DI
- B-07350041580966 EUDAMED
- EMDN Code
- M03020202 MEDICATED BANDAGES, WITH ZINC OXIDE AND AMMONIUM BITUMINOSULFONATE EUDAMED
Classification
- Device Class
- Class III EUDAMED
- Market of Registration
- Sweden EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Implantable
No
EUDAMED
Reusable
No
EUDAMED
Contains Latex
No
EUDAMED
Reprocessed
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
Yes
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
Yes
EUDAMED
Ichthopaste by Evolan Pharma AB — Class III — MDD — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/MDD
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | B-07350041580966 | Class III | Active |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Evolan Pharma AB
- EUDAMED SRN
- SE-MF-000004426
Sources (1)
- EUDAMED 1e531ba1-15a5-43f7-87ab-03905518536a 61 fields · synced Jun 18, 2026