Kindersicher T.O. Zugck
DE-MF-000005315 · Germany · Heide
Kindersicher T.O. Zugck is registered in the European database on medical devices as a manufacturer, with 9 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 9 |
|---|
Most frequent device types declared: Kindersicher Infoflip deutsch.
Devices declared under this manufacturer
- Enfant Securite, Echelle de couleur KINDERSICHER, édition suisse franç
- Enfant Securite, Infoflip Französisch
- Farbcodiertes Kindersicher Maßband deutsch
- Infoflip Kindersicher Schweiz
- Infoflip Kindersicher Schweiz/Französisch Ch/F
- Infoflip Kindersicher Österreich
- Infoflip Kindersicher-System
- Kindersicher.me
- Kindersicher.me farbcodiertes Broselow Kindermaßband
Catalogue references include IF KiSi Ch/D Schweiz, IF KiSi Ch/F Französisch, IF KiSi Französisch Enfant Securite, IF KiSi Österreich, KiSi IF deutsch, KiSi MB deutsch.
European nomenclature codes declared: L1699.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 9 |
| Country of registration | Germany |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 9 |
|---|---|
| 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. Kindersicher T.O. Zugck was not found in either the U.S. or the Canadian register.