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EUDAMED registration 06931377228992No

ECG cables with lead wires

Shenzhen Amydi-med Electrics Tech Co.,LtdClass IEU EUDAMEDTrade name: ECG Cable with Lead wires
VerifiedEUDAMED · official EU database
Device classification
Risk class
Class I
CND nomenclatures code
Z1203020285
Trade name
ECG Cable with Lead wires
Implantable
No
Reusable
No
Measuring function
No
Registration information
Primary DI
06931377228992
Basic UDI
69313772808UY
Active status
No
Manufacturer
Manufacturer name
Shenzhen Amydi-med Electrics Tech Co.,Ltd
Country
China
Country type
NON_EU
Address
601,No.15 Building,Xianan No. 3 Industrial Zone Shangcun, Gongming Street, Guangming District, Shenzhen, Guangdong Shenzhen
Email
sales@amydi-med.com
Authorized representative
Name
Umedwings Netherlands B.V.
SRN
NL-AR-000000444
Country
Netherlands
Address
Treubstraat 1 Rijswijk
Email
ar@umedwings.eu
Telephone
+31 (0) 642758955
Regulatory information
Competent authority
Ministerie van Volksgezondheid, Welzijn en Sport
Applicable legislation
MDR (REGULATION (EU) 2017/745 on medical devices)
Placed on the market
Denmark
Market available
Denmark:None~None, France:None~None, Germany:None~None, Netherlands:None~None, Poland:None~None, Sweden:None~None
Device characteristics
Human tissues
No
Animal tissues
No
Device description (EMDN)

MULTI-PARAMETER MONITORS - CONSUMABLES

About this record

Access comprehensive regulatory information for ECG cables with lead wires 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 06931377228992 and manufactured by Shenzhen Amydi-med Electrics Tech Co.,Ltd in China.

This page provides complete registration details including trade name (ECG Cable with Lead wires), 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.