Cross linked 2
- Risk class
- Class IIa
- CND nomenclatures code
- Q010699
- Trade name
- Cross linked 2
- Implantable
- No
- Reusable
- No
- Measuring function
- No
- Primary DI
- +EPOLCLI7B20O
- Basic UDI
- ++EPOLAPTKB
- Active status
- No
- Manufacturer name
- Polident d.o.o. Industrija dentalnih proizvodov
- Country
- Slovenia
- Country type
- EU_MEMBER_STATE
- Address
- 42 Volcja Draga Volcja Draga
- polident@polident.si
- Competent authority
- Javna agencija Republike Slovenije za zdravila in medicinske pripomočke.
- Applicable legislation
- MDR (REGULATION (EU) 2017/745 on medical devices)
- Placed on the market
- Slovenia
- Market available
- Austria:None~None, Belgium:None~None, Bulgaria:None~None, Croatia:None~None, Cyprus:None~None, Czechia:None~None, Denmark:None~None, Estonia:None~None, Finland:None~None, France:None~None, Germany:None~None, Greece:None~None, Hungary:None~None, Iceland:None~None, Ireland:None~None, Italy:None~None, Latvia:None~None, Liechtenstein:None~None, Lithuania:None~None, Luxembourg:None~None, Malta:None~None, Netherlands:None~None, Norway:None~None, Poland:None~None, Portugal:None~None, Romania:None~None, Slovakia:None~None, Slovenia:None~None, Spain:None~None, Sweden:None~None, Türkiye:None~None, United Kingdom (Northern Ireland only):None~None
- Human tissues
- No
- Animal tissues
- No
MATERIALS FOR THE PREPARATION OF CUSTOM-MADE DENTAL DEVICES - OTHER
Access comprehensive regulatory information for Cross linked 2 in the European Union medical device market through Pure Global AI's free database. This Class IIa device is registered with EU EUDAMED under Primary DI +EPOLCLI7B20O and manufactured by Polident d.o.o. Industrija dentalnih proizvodov in Slovenia.
This page provides complete registration details including trade name (Cross linked 2), manufacturer information, competent authority (Javna agencija Republike Slovenije za zdravila in medicinske pripomočke.), and regulatory compliance data from the official EU EUDAMED medical device database. Pure Global AI offers free access to the European Union's complete medical device registry, helping global MedTech companies navigate EU MDR regulations efficiently.