EUDAMED registration 08964003475734NoSterilizing needle box no.3
- Risk class
- Class I
- CND nomenclatures code
- L0203
- Trade name
- Sterilizing needle box no.3
- Implantable
- No
- Reusable
- Yes
- Measuring function
- No
- Primary DI
- 08964003475734
- Basic UDI
- 08964003475STZB03F9
- Version date
- September 02, 2024
- Manufacturer last update
- December 01, 2022
- Active status
- No
- Manufacturer name
- JAZBAR INTERNATIONAL
- Country
- Pakistan
- Country type
- NON_EU
- Address
- CAPITAL ROAD DEEN PURA SIALKOT
- jazbarinternational@gmail.com
- SRN
- HU-AR-000034102
- Country
- Hungary
- Address
- 13. al. 1 Budapest, Auróra utca BUDAPEST
- eudamed.representative@gmail.com
- Telephone
- +36706790786
- Competent authority
- Danish Medicines Agency, Pharmacovigilance & Medical Devices
- Applicable legislation
- MDR (REGULATION (EU) 2017/745 on medical devices)
- Placed on the market
- Romania
- Market available
- 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, Austria:None~None
- Human tissues
- No
- Animal tissues
- No
NEEDLE CONTAINERS, REUSABLE
Access comprehensive regulatory information for Sterilizing needle box no.3 in the European Union medical device market through Pure Global AI's free database. This Class I device is registered with EU EUDAMED under Primary DI 08964003475734 and manufactured by JAZBAR INTERNATIONAL in Pakistan.
This page provides complete registration details including trade name (Sterilizing needle box no.3), manufacturer information, authorized representative details, competent authority (Danish Medicines Agency, Pharmacovigilance & Medical Devices), 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.