Devices (same UDI-DI)
1
Certificates
3
Countries
9
Notified Bodies
3
Basic Information
- Primary DI
- 17350030052150
- Basic UDI-DI Code
- B-17350030052150
- Reference
- -
- Device Types
-
Single use Sterile
- Regulation
- Eu Mdd
- Classification
- Eu Md Class 3
- Status
- On The Market
- Manufacturer
- Bohus BioTech AB
Additional Description
Z każdą strzykawką dostarczane są dwie jednorazowe sterylne igły. Informacje o rozmiarze igły i metodzie sterylizacji można znaleźć na zewnętrznej części opakowania igły. Objętość każdej igły jest wskazana na opakowaniu zewnętrznym. Do każdego opakowania są załączone etykiety do wpisania danych pacjenta, aby zapewnić identyfikację produktu.
CND Nomenclature Codes
| Code | Description |
|---|---|
| P900402 | RESORBABLE FILLING AND RECONSTRUCTION DEVICES |
Certificates
| Type | Number | Notified Body | Status |
|---|---|---|---|
| MDD Annex II (excluding section 4) | D1001800117 | MDC MEDICAL DEVICE CERTIFICATION GMBH | Expired |
| MDD Annex II Section 4 | D1001800093 | MDC MEDICAL DEVICE CERTIFICATION GMBH | Expired |
| MDD Annex II (excluding section 4) | D1001800076 | MDC MEDICAL DEVICE CERTIFICATION GMBH | Expired |
Available In Countries
🇧🇬 Bulgaria
🇨🇾 Cyprus
🇪🇸 Spain
🇭🇺 Hungary
🇵🇱 Poland
🇵🇹 Portugal
🇷🇴 Romania
🇸🇪 Sweden
🇹🇷 Türkiye
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