Lambotte bone holding forcep 30cm
- Risk class
- Class I
- CND nomenclatures code
- L03130499
- Trade name
- Lambotte bone holding forcep 30cm
- Implantable
- No
- Reusable
- Yes
- Measuring function
- No
- Primary DI
- 08961103944115
- Basic UDI
- 896110394Bi8-622F4
- Active status
- No
- Manufacturer name
- Battan International
- Country
- Pakistan
- Country type
- NON_EU
- Address
- Noul More, Wazirabad Road, Sialkot
- battaninternational@gmail.com
- SRN
- HU-AR-000034102
- Country
- Hungary
- Address
- 13. al. 1 Budapest, Auróra utca BUDAPEST
- eudamed.representative@gmail.com
- Telephone
- +36706790786
- Competent authority
- Nemzeti Népegészségügyi és Gyógyszerészeti Központ
- Applicable legislation
- MDR (REGULATION (EU) 2017/745 on medical devices)
- Placed on the market
- Spain
- 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
GRASPING FORCEPS, REUSABLE - OTHER
Access comprehensive regulatory information for Lambotte bone holding forcep 30cm 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 08961103944115 and manufactured by Battan International in Pakistan.
This page provides complete registration details including trade name (Lambotte bone holding forcep 30cm), manufacturer information, authorized representative details, competent authority (Nemzeti Népegészségügyi és Gyógyszerészeti Központ ), 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.