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EUDAMED registration 06974957360712No

OPHTHALMIC FORCEPS

GAUSH PRECISION LTDClass IEU EUDAMEDTrade name: OPHTHALMIC FORCEPS(needle holder)
VerifiedEUDAMED · official EU database
Device classification
Risk class
Class I
CND nomenclatures code
Q021102
Trade name
OPHTHALMIC FORCEPS(needle holder)
Implantable
No
Reusable
No
Measuring function
No
Registration information
Primary DI
06974957360712
Basic UDI
697495736ED001K9
Version date
February 21, 2025
Manufacturer last update
December 25, 2024
Active status
No
Manufacturer
Manufacturer name
GAUSH PRECISION LTD
Country
China
Country type
NON_EU
Address
Room 201,Building 8,No.188 Fuchunjiang Road,HuQiu District Suzhou City
Email
szra@gaush.com
Authorized representative
Name
RIOMAVIX SOCIEDAD LIMITADA
SRN
ES-AR-000001202
Country
Spain
Address
55 Calle de Almansa Madrid
Email
leis@riomavix.com
Regulatory information
Competent authority
Agencia Española de Medicamentos y Productos Sanitarios
Applicable legislation
MDR (REGULATION (EU) 2017/745 on medical devices)
Placed on the market
Germany
Device characteristics
Human tissues
No
Animal tissues
No
Device description (EMDN)

OPHTHALMIC SURGERY FORCEPS, SINGLE-USE

About this record

Access comprehensive regulatory information for OPHTHALMIC FORCEPS 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 06974957360712 and manufactured by GAUSH PRECISION LTD in China.

This page provides complete registration details including trade name (OPHTHALMIC FORCEPS(needle holder)), manufacturer information, authorized representative details, competent authority (Agencia Española de Medicamentos y Productos Sanitarios), 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.