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EUDAMED registration 06971042225024No

6 RP Panel I

SHANGHAI ZJ BIO-TECH CO., LTDIVD GeneralEU EUDAMEDTrade name: 6 RP Panel I
VerifiedEUDAMED · official EU database
Device classification
Risk class
IVD General
CND nomenclatures code
W0105070304
Trade name
6 RP Panel I
Implantable
No
Reusable
No
Measuring function
No
Registration information
Primary DI
06971042225024
Basic UDI
B-06971042225024
Version date
October 17, 2024
Manufacturer last update
September 01, 2022
Active status
No
Manufacturer
Manufacturer name
SHANGHAI ZJ BIO-TECH CO., LTD
Country
China
Country type
NON_EU
Address
528 Ruiqing Road No. 20 and 21 Building, 528 Ruiqing Road, Zhangjiang High-tech Industrial East District Shanghai
Email
registration@liferiver.com.cn
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
Federaal Agentschap voor Geneesmiddelen en Gezondheidsproducten/ Afdeling Gezondheidsproducten
Applicable legislation
IVDD (Directive 98/79/EC on in vitro Diagnostic Medical Devices)
Placed on the market
France
Device characteristics
Human tissues
No
Animal tissues
No
Device description (EMDN)

INFLUENZA & PARA INFLUENZA / RESPIRATORY SYNCYTIAL VIRUS (RSV) - MULTIPLEX NA REAGENTS

About this record

Access comprehensive regulatory information for 6 RP Panel I in the European Union medical device market through Pure Global AI's free database. This IVD General device is registered with EU EUDAMED under Primary DI 06971042225024 and manufactured by SHANGHAI ZJ BIO-TECH CO., LTD in China.

This page provides complete registration details including trade name (6 RP Panel I), manufacturer information, authorized representative details, competent authority (Federaal Agentschap voor Geneesmiddelen en Gezondheidsproducten/ Afdeling Gezondheidsproducten), 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.