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Gigle Handle - EUDAMED Registration G410M19037010

Access comprehensive regulatory information for Gigle Handle 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 G410M19037010 and manufactured by MEHRISH INDUSTRIES PVT LTD in Pakistan.

This page provides complete registration details including trade name (Gigle Handle), 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.

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EUDAMED Official Data
Class I
G410M19037010
No
Gigle Handle
Trade Name: Gigle Handle
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Device Description (EMDN)

SURGICAL KNIVES, REUSABLE

Device Classification
Risk Class
Class I
CND Nomenclatures Code
L0102
Trade Name
Gigle Handle
Implantable
No
Reusable
Yes
Measuring Function
No
Registration Information
Primary DI
G410M19037010
Basic UDI
++G410M1903701UA
Version Date
December 28, 2024
Manufacturer Last Update
December 02, 2022
Active Status
No
Manufacturer
Country
Pakistan
Country Type
NON_EU
Address
86 B-Industrial Estate, Sialkot
Email
mehrish@mehrish.com
Authorized Representative
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
Romania
Device Characteristics
Human Tissues
No
Animal Tissues
No