Identity
- Trade Name
- AKUTOL™ odstraňovač náplastí sprej EUDAMED
- Device Name
- AKUTOL™ Odstraňovač náplastí sprej EUDAMED
- Model / Reference
- Z300000 EUDAMEDZ36 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 08594013705288 EUDAMED08594013703963 EUDAMED
- Basic UDI-DI
- 859401370Z30NB EUDAMED
- EMDN Code
- M9003 SOLUTIONS FOR ADHESIVE TAPE REMOVAL EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- Czechia 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
AKUTOL™ odstraňovač náplastí sprej by AVEFLOR, a.s. — 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 | 859401370Z30NB | Class I | Active |
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Manufacturer
- Manufacturer
- AVEFLOR, a.s.
- EUDAMED SRN
- CZ-MF-000003103
Sources (2)
- EUDAMED 4480a855-7f55-4a3e-a59c-239fc71e4fd9 61 fields · synced Jul 14, 2026
- EUDAMED 8e21703c-2b11-41b4-8d5f-1cb45b39fc47 61 fields · synced May 17, 2026