Waldemar Knittel Glasbearbeitungs GmbH
DE-MF-000005025 · Germany · Braunschweig
Waldemar Knittel Glasbearbeitungs GmbH is registered in the European database on medical devices as a manufacturer, with 30 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
Devices declared under this manufacturer
- KT Premium Adhesion Microscope Slides
- KT Premium Adhesion Microscope Slides for Ink Printers
- KT Premium Adhesion Supa Mega Microscope Slides
- KT Premium Non-Adhesion Microscope Slides
- KT Premium Non-Adhesion Microscope Slides for Ink Printers
- KT Premium Non-Adhesion Supa Mega Microscope Slides
- KT-Premium Cover Glass
- KT-Premium Supa Mega Cover Glass
- Knittel Glass Cover Glass
- Knittel Glass Microscope Slides
- Knittel Glass Starfrost Microscope Slides
Showing 12 of 30 declared devices.
Catalogue references include CD12432Y3D.01 , KT-10-2432, CS112741FKC.01 , JKA61205, KT-15-2232, KT-15-2250, KT1-I-WH-90, KT1-I-WH-CL.
European nomenclature codes declared: W0503900201, W0503900202.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | Waldemar Knittel Glasbearbeitungs GmbH (DE) · FDA 1000469910 |
| Devices in EUDAMED | 30 |
| Country of registration | Germany |
Device-level evidence
| Devices with a numeric GTIN | 30 |
|---|---|
| Found in the U.S. device database | 6 |
| Share | 20.0 % |
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: United States only. Waldemar Knittel Glasbearbeitungs GmbH is registered in the United States but was not found in the Canadian register.