Berchtold GmbH & Co. KG
DE-MF-000005446 · Germany · Tuttlingen
Berchtold GmbH & Co. KG is registered in the European database on medical devices as a manufacturer, with 6 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 6 |
|---|
Most frequent device types declared: 08858250000749SL, 08858250000753SB, 08858251028124U5.
Among these devices, 6 are declared active.
Devices declared under this manufacturer
- Chromophare
- Oculan
- Operon
Catalogue references include CH00000001, COMM0001, COMM0002, COMM0003, COMM0004, OPE10000.
European nomenclature codes declared: Z12010702, Z129004, Z12011202.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | BERCHTOLD GMBH & CO. KG (DE) · FDA 8010153 |
| Devices in EUDAMED | 6 |
| Country of registration | Germany |
Device-level evidence
| Devices with a numeric GTIN | 6 |
|---|---|
| Found in the U.S. device database | 1 |
| Share | 16.7 % |
Canadian market access
| Health Canada licence listing | Licensed in Canada |
|---|---|
| Matched entry | BERCHTOLD GMBH & CO. KG |
North American profile: Both markets. Berchtold GmbH & Co. KG is registered in both the United States and Canada.