- Role
- Country
- Date of registration
- Address
EUDAMED last updated this device on Feb 12, 2024
8710103BM782K2NIPPLESHIELD is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by Philips Consumer Lifestyle B.V.. Placed on the EU market in Croatia. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
087101039150898710103BM782K2SCF153/13(01)08710103915089
The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
European Medical Device Nomenclature — the EU product classification assigned to this device.
U1003PUERPERIUM DEVICESNo certificate specifically references this device's Basic UDI-DI.
Primary placement in Croatia; available across 13 countries total.
| Country | On market since | Until |
|---|---|---|
| CroatiaPrimary placement | Apr 21, 2021 | Dec 31, 9999 |
| Austria | Still on market | |
| Belgium | Still on market | |
| Czechia | Still on market | |
| Spain | Still on market | |
| France | Still on market | |
| Hungary | Still on market | |
| Italy | Still on market | |
| Netherlands | Still on market | |
| Poland | Still on market | |
| Portugal | Still on market | |
| Slovakia | Still on market | |
| Slovenia | Apr 21, 2021 | Dec 31, 9999 |
NL-MF-000001693No certificates registered for this manufacturer.
No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.