Philips Medical Systems Nederland B.V.
NL-MF-000023083 · Netherlands · Eindhoven
Philips Medical Systems Nederland B.V. 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: 1.0, 5.
Among these devices, 5 are declared active.
Devices declared under this manufacturer
- Health Informatics Suite Clinical Decision Support B
- Health Informatics Suite, version 5
- Tasy EMR, version 3.07
- Tasy EMR, version 4
- Tasy EMR, version 5
- Virtual Acute Care, Version 1.00
Catalogue references include 756003, 756011, 756025, 837002.
European nomenclature codes declared: V92.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | Philips Medical Systems Nederland B.V. (NL) · FDA 3015777306 |
| Devices in EUDAMED | 6 |
| Country of registration | Netherlands |
Device-level evidence
| Devices with a numeric GTIN | 6 |
|---|---|
| Found in the U.S. device database | 0 |
| Share | 0.0 % |
Canadian market access
| Health Canada licence listing | Licensed in Canada |
|---|---|
| Matched entry | PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. |
What it holds in Canada
| Licences on record | 106 |
|---|---|
| Currently active | 0 |
| Class 2 devices | 72 |
| Class 3 devices | 34 |
| First licensed | 1999-11-10 |
Licence types: System (53), Single Device (30), Device Family (21), Device Group Family (1).
Licensed under: ADVANCED VISUALIZATION WORKSPACE, NM SUITE, SPECTRAL CT 7500 RT, AV VIEWER, AV CARDIOVASCULAR SUITE, INTEGRIS VASCULAR IMAGING SYSTEMS.
North American profile: Both markets. Philips Medical Systems Nederland B.V. is registered in both the United States and Canada.