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EUDAMED registration G520MD45030No

Gingras Ligature Director

MedspoClass IEU EUDAMEDTrade name: Gingras Ligature Director
VerifiedEUDAMED · official EU database
Device classification
Risk class
Class I
CND nomenclatures code
L150701
Trade name
Gingras Ligature Director
Implantable
No
Reusable
Yes
Measuring function
No
Registration information
Primary DI
G520MD45030
Basic UDI
++G520MD4503L7
Version date
March 30, 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)

ORTHODONTIC LIGATURE TOOLS, REUSABLE

About this record

Access comprehensive regulatory information for Gingras Ligature Director 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 G520MD45030 and manufactured by Medspo in Pakistan.

This page provides complete registration details including trade name (Gingras Ligature Director), 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.