Pure Global AI
EUDAMED registration 08964003475741No

sterilizing endo box

JAZBAR INTERNATIONALClass IEU EUDAMEDTrade name: sterilizing endo box
VerifiedEUDAMED · official EU database
Device classification
Risk class
Class I
CND nomenclatures code
S010499
Trade name
sterilizing endo box
Implantable
No
Reusable
Yes
Measuring function
No
Registration information
Primary DI
08964003475741
Basic UDI
08964003475STEB04AQ
Version date
September 02, 2024
Manufacturer last update
December 01, 2022
Active status
No
Manufacturer
Manufacturer name
JAZBAR INTERNATIONAL
Country
Pakistan
Country type
NON_EU
Address
CAPITAL ROAD DEEN PURA SIALKOT
Email
jazbarinternational@gmail.com
Authorized representative
Name
KHANG BAO INTERNATIONAL KFT
SRN
HU-AR-000034102
Country
Hungary
Address
13. al. 1 Budapest, Auróra utca BUDAPEST
Email
eudamed.representative@gmail.com
Telephone
+36706790786
Regulatory information
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
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
Device characteristics
Human tissues
No
Animal tissues
No
Device description (EMDN)

STERILISATION CONTAINERS - OTHER

About this record

Access comprehensive regulatory information for sterilizing endo box 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 08964003475741 and manufactured by JAZBAR INTERNATIONAL in Pakistan.

This page provides complete registration details including trade name (sterilizing endo box), 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.