KiiltoClean Oy
FI-MF-000001622 · Finland · Turku
KiiltoClean Oy is registered in the European database on medical devices as a manufacturer, with 41 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 41 |
|---|
Devices declared under this manufacturer
- Alu Deko 200L
- Antibac Overflatedesinfeksjon Premium 88,8% 750 ml
- Antibac Overflatedesinfeksjon+ 75% m. tensid 750 ml
- Deko 5L
- Erinox 1L
- Erinox 200L
- Erizyme 200L
- Erizyme 5L
- Kiilto Pro Easydes 5 l
- Kiilto Pro Easydes 500 ml
- Kiilto Pro Easydes Wipes 16 pcs
- Kiilto Pro Erisan Des 3 l
Showing 12 of 41 declared devices.
Catalogue references include 8081, 8083, 8113, 8126, 8143, 8148.
European nomenclature codes declared: D0701, D0899, D0902, D0702, D050101, D0801.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 41 |
| Country of registration | Finland |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 41 |
|---|---|
| Found in the U.S. device database | 0 |
| Share | 0.0 % |
Canadian market access
| Health Canada licence listing | Not found in the Canadian register |
|---|
⚠️ Canada lists no Class I devices at all — what that excludes.
North American profile: Neither register. KiiltoClean Oy was not found in either the U.S. or the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
CR-03-1201-785-22 | issued | 2027-05-11 |