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EUDAMED registration 06975141982147No

Nucleic Acid Purification System

HANGZHOU ALLSHENG INSTRUMENTS CO.,LTDClass AEU EUDAMEDTrade name: Nucleic Acid Purification System
VerifiedEUDAMED · official EU database
Device classification
Risk class
Class A
CND nomenclatures code
W0299
Trade name
Nucleic Acid Purification System
Implantable
No
Reusable
No
Measuring function
No
Registration information
Primary DI
06975141982147
Basic UDI
697514198AS154FE
Version date
October 10, 2024
Manufacturer last update
February 18, 2022
Active status
No
Manufacturer
Manufacturer name
HANGZHOU ALLSHENG INSTRUMENTS CO.,LTD
Country
China
Country type
NON_EU
Address
No.7 of Zhuantang Science and Technology Economic Zone Hangzhou City
Email
tuyx@allsheng.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
IVDR (REGULATION (EU) 2017/746 on in vitro diagnostic medical devices)
Placed on the market
France
Market available
France:2024-10-12~2030-10-12, Italy:2024-10-12~2030-10-12, Spain:2024-10-12~2030-10-12
Device characteristics
Human tissues
No
Animal tissues
No
Device description (EMDN)

IVD INSTRUMENTS - OTHER

About this record

Access comprehensive regulatory information for Nucleic Acid Purification System in the European Union medical device market through Pure Global AI's free database. This Class A device is registered with EU EUDAMED under Primary DI 06975141982147 and manufactured by HANGZHOU ALLSHENG INSTRUMENTS CO.,LTD in China.

This page provides complete registration details including trade name (Nucleic Acid Purification System), 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.