Pure Global AI
EUDAMED registration 06975871860463No

Reusable pressure infusor

Ningbo KK-Bioscience Co., Ltd.Class IEU EUDAMED
VerifiedEUDAMED · official EU database
Device classification
Risk class
Class I
CND nomenclatures code
B0499
Implantable
No
Reusable
No
Measuring function
No
Registration information
Primary DI
06975871860463
Basic UDI
697587186RIB001TP
Version date
April 11, 2024
Manufacturer last update
November 23, 2021
Active status
No
Manufacturer
Manufacturer name
Ningbo KK-Bioscience Co., Ltd.
Country
China
Country type
NON_EU
Address
38 #38, Dongzhou Industrial Park, Xi`dian Town, Ningbo
Email
sales@kk-bioscience.com
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
MDR (REGULATION (EU) 2017/745 on medical devices)
Placed on the market
Italy
Device characteristics
Human tissues
No
Animal tissues
No
Device description (EMDN)

AUTOTRANSFUSION DEVICES - OTHER

About this record

Access comprehensive regulatory information for Reusable pressure infusor 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 06975871860463 and manufactured by Ningbo KK-Bioscience Co., Ltd. in China.

This page provides complete registration details including 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.