Philips Consumer Lifestyle B.V.
NL-MF-000001693 · Netherlands · Drachten
Philips Consumer Lifestyle B.V. is registered in the European database on medical devices as a manufacturer, with 57 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 57 |
|---|
Among these devices, 38 are declared active.
Devices declared under this manufacturer
- BREASTSHELLSET
- NIPLETTE
- NIPPLE SHIELD
- NIPPLESHIELD
Showing 12 of 57 declared devices.
Catalogue references include BRC333, BRI934, BRI938, SCF152/01, SCF153/01, SCF153/13.
European nomenclature codes declared: Z12040201, U1003, Z12080303.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | Philips Consumer Lifestyle B.V. (NL) · FDA 3010359222 |
| Devices in EUDAMED | 57 |
| Country of registration | Netherlands |
Device-level evidence
| Devices with a numeric GTIN | 57 |
|---|---|
| Found in the U.S. device database | 0 |
| Share | 0.0 % |
Canadian market access
| Health Canada licence listing | Similar name found — unverified |
|---|---|
| Matched entry | PHILIPS CONSUMER LIFESTYLE BV |
⚠️ A similar name exists; unverified — why.
What it holds in Canada
| Licences on record | 1 |
|---|---|
| Currently active | 0 |
| Class 2 devices | 1 |
| First licensed | 2020-06-04 |
Licence types: Device Family (1).
Licensed under: PHILIPS AVENT SINGLE/DOUBLE ELECTRIC BREAST PU.