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NIBP CUFF - EUDAMED Registration 06972820962643

Access comprehensive regulatory information for NIBP CUFF 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 06972820962643 and manufactured by Shenzhen SINO-K Medical Technology Co., Ltd. in China.

This page provides complete registration details including trade name (SC1711), manufacturer information, authorized representative details, competent authority (DE/CA20, Bezirksregierung Düsseldorf Dezernat 24), 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.

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EUDAMED Official Data
Class I
06972820962643
No
NIBP CUFF
Trade Name: SC1711
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Device Description (EMDN)

GENERAL MEDICINE DIAGNOSIS AND MONITORING INSTRUMENTS - CONSUMABLES

Device Classification
Risk Class
Class I
CND Nomenclatures Code
Z12040185
Trade Name
SC1711
Implantable
No
Reusable
Yes
Measuring Function
Yes
Registration Information
Primary DI
06972820962643
Basic UDI
B-06972820962643
Version Date
August 30, 2024
Manufacturer Last Update
March 08, 2022
Active Status
No
Manufacturer
Country
China
Country Type
NON_EU
Address
Room 401, Bldg 2, Veteran Ind. City, Gongle Community, Xixiang Street, Baoan District Shenzhen
Email
huaweiyin@sino-k.com
Authorized Representative
SRN
DE-AR-000005129
Country
Germany
Address
56 Brehmstr Düsseldorf
Email
med@eulinx.eu
Telephone
+4921131054698
Regulatory Information
Competent Authority
DE/CA20, Bezirksregierung Düsseldorf Dezernat 24
Applicable Legislation
MDD (Directive 93/42/EEC on Medical Devices)
Placed On The Market
Ireland
Device Characteristics
Human Tissues
No
Animal Tissues
No