C. H. Müller Industries GmbH
DE-MF-000027887 · Germany · Heinsdorfergrund
C. H. Müller Industries GmbH is registered in the European database on medical devices as a manufacturer, with 8 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 8 |
|---|
Among these devices, 8 are declared sterile.
Devices declared under this manufacturer
- Stertouch Pro CHM BS01 380-Rx290
- Stertouch Pro CHM BS02 419-Rx290
- Stertouch Pro CHM D24-OS 580-Rx420
- Stertouch Pro CHM D27 700-Rx480
- Stertouch Pro CHM SC13 330-Rx260
- Stertouch Pro KS 21.5Z 540-Rx375
- Stertouch Pro KS 24Z 610-Rx415
- Stertouch Pro KS 27Z 700-Rx480
Catalogue references include FW26280, FW26281, FW26287, FW26288, FW26301, FW26374.
European nomenclature codes declared: T030199.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 8 |
| 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 | 8 |
|---|---|
| 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. C. H. Müller Industries GmbH was not found in either the U.S. or the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
G15 105412 0004 | issued | 2028-04-11 |