Philips Medical Systems DMC GmbH
DE-MF-000005362 · Germany · Hamburg
Philips Medical Systems DMC GmbH is registered in the European database on medical devices as a manufacturer, with 263 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIb | 212 |
|---|---|
| Class IIa | 51 |
Among these devices, 160 are declared active.
Devices declared under this manufacturer
- Anti-scatter Grid (36/12/100)
- Anti-scatter Grid (36/12/180)
- CTR1740
- CTR2150CESV
- CTR2250
- CTR2251
- CTR2280
- Console Trolley
- MRM 0410 ROT-GS 2502
- Monitor CS for 2 Monitors (Eth)
- REEVO240G
- SRO 2550 ROT 360
Showing 12 of 263 declared devices.
Catalogue references include 451220112381, 451220203321, 451220203341, 459800498411, 459800559451, 459800730271.
European nomenclature codes declared: Z11039012, Z11039080, Z11039011, Z11039099, Z11039009, Z11039016.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | Philips Medical Systems DMC GmbH (DE) · FDA 3003768251 |
| Devices in EUDAMED | 263 |
| Country of registration | Germany |
Device-level evidence
| Devices with a numeric GTIN | 263 |
|---|---|
| Found in the U.S. device database | 210 |
| Share | 79.8 % |
Canadian market access
| Health Canada licence listing | Licensed in Canada |
|---|---|
| Matched entry | PHILIPS MEDICAL SYSTEMS DMC GMBH |
What it holds in Canada
| Licences on record | 26 |
|---|---|
| Currently active | 0 |
| Class 2 devices | 19 |
| Class 3 devices | 7 |
| First licensed | 1998-12-18 |
Licence types: Single Device (14), System (6), Device Family (5), Device Group (1).
Licensed under: PHILIPS DUO DIAGNOST, DIGITAL DIAGNOST, BUCKY DIAGNOST, X-RAY GENERATORS, EASY DIAGNOST RADIOGRAPHIC/FLUOROSCOPIC EQUIPM, X-RAY TUBE HOUSING ASSEMBLIES.
North American profile: Both markets. Philips Medical Systems DMC GmbH is registered in both the United States and Canada.