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EUDAMED registration G520MD10960No

Extraction Forceps Fig 79

MedspoClass IEU EUDAMEDTrade name: Extraction Forceps Fig 79
VerifiedEUDAMED · official EU database
Device classification
Risk class
Class I
CND nomenclatures code
L150301
Trade name
Extraction Forceps Fig 79
Implantable
No
Reusable
Yes
Measuring function
No
Registration information
Primary DI
G520MD10960
Basic UDI
++G520MD1096KS
Version date
September 10, 2024
Manufacturer last update
September 14, 2023
Active status
No
Manufacturer
Manufacturer name
Medspo
Country
Pakistan
Country type
NON_EU
Address
01, New Miana Pura East,, Muhammadi Railway Crossing,, Sialkot. Sialkot
Email
hbilalsiddiqui@gmail.com
Authorized representative
Name
ANTEX MEDI SOLUTION
SRN
DE-AR-000008078
Country
Germany
Address
6 Hans Bunte Strasse Heidelberg
Email
info@antex-medi-solution.de
Telephone
+4915678612574
Regulatory information
Competent authority
DE/CA38 - Regierungspräsidium Karlsruhe
Applicable legislation
MDR (REGULATION (EU) 2017/745 on medical devices)
Placed on the market
Germany
Market available
Germany:None~None, Italy:None~None
Device characteristics
Human tissues
No
Animal tissues
No
Device description (EMDN)

DENTAL EXTRACTION TOOTH FORCEPS, REUSABLE

About this record

Access comprehensive regulatory information for Extraction Forceps Fig 79 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 G520MD10960 and manufactured by Medspo in Pakistan.

This page provides complete registration details including trade name (Extraction Forceps Fig 79), manufacturer information, authorized representative details, competent authority (DE/CA38 - Regierungspräsidium Karlsruhe), 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.