Identity
- Trade Name
- Kiilto Pro Erisan Des 500 ml EUDAMED
- Device Name
- Kiilto Pro Erisan Des EUDAMEDKiilto Pro Erisan Des 500 ml EUDAMED
- Model / Reference
- 8126 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 06417964081268 EUDAMED
- Basic UDI-DI
- 6417964MDL031013808U EUDAMEDB-06417964081268 EUDAMED
- EMDN Code
- D0902 ASSOCIATED AMMONIUM SALTS FOR THE DISINFECTION OF MEDICAL DEVICES EUDAMED
Classification
- Device Class
- Class IIa EUDAMED
- Market of Registration
- Finland 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
Kiilto Pro Erisan Des 500 ml by KiiltoClean Oy — Class IIa — MDD, MDR — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/MDD
European Union Active
CE/MDR
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | 6417964MDL031013808U | Class IIa | Active |
| EUDAMED | European Union | CE/MDR | 6417964MDL031013808U | Class IIa | Active |
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Manufacturer
- Manufacturer
- KiiltoClean Oy
- EUDAMED SRN
- FI-MF-000001622
Sources (2)
- EUDAMED 5318af3e-deb9-4172-b6cc-8eb1fc840792 61 fields · synced Jun 18, 2026
- EUDAMED 521bf43b-32c1-4ec3-9238-2d9b3ba1e4cf 61 fields · synced May 19, 2026