EUDAMED registration 06973094411585No

Cell Preservative Fluid

Name: Cell Preservative Fluid — EUDAMED registration 06973094411585
Creator: Junocare Medical Devices Ltd
Keywords: Cell Preservative Fluid, 06973094411585, Cell Preservative Fluid, Class I, Junocare Medical Devices Ltd, EUDAMED registration

Junocare Medical Devices LtdClass IEU EUDAMEDTrade name: Cell Preservative Fluid

VerifiedEUDAMED · official EU database

Device classification

Risk class: Class I
CND nomenclatures code: W01019099
Trade name: Cell Preservative Fluid
Implantable: No
Reusable: No
Measuring function: No

Registration information

Primary DI: 06973094411585
Basic UDI: B-06973094411585
Version date: January 17, 2024
Manufacturer last update: November 14, 2022
Active status: No

Manufacturer

Manufacturer name: Junocare Medical Devices Ltd
Country: China
Country type: NON_EU
Address: BLOCK 13, LIANDO U VALLEY BEIJING
Email: lijinli@amberdale.cn

Authorized representative

Name: Humiss International B.V.
SRN: NL-AR-000001490
Country: Netherlands
Address: 701 Joop Geesinkweg Amsterdam-Duivendrech
Email: ce-tech@humiss.com
Telephone: +31 (0)20 369 8116

Regulatory information

Competent authority: Ministerie van Volksgezondheid, Welzijn en Sport
Applicable legislation: MDD (Directive 93/42/EEC on Medical Devices)
Placed on the market: Greece
Market available: Austria:None~None, Belgium:None~None, Denmark:None~None, France:None~None, Greece:None~None, Italy:None~None, Netherlands:None~None, Norway:None~None, Turkey:None~None

Device characteristics

Human tissues: No
Animal tissues: No

Device description (EMDN)

CLINICAL CHEMISTRY REAGENTS - OTHER

About this record

Access comprehensive regulatory information for Cell Preservative Fluid 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 06973094411585 and manufactured by Junocare Medical Devices Ltd in China.

This page provides complete registration details including trade name (Cell Preservative Fluid), manufacturer information, authorized representative details, competent authority (Ministerie van Volksgezondheid, Welzijn en Sport), 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.