Pure Global AI
EUDAMED registration 06931038631031No

stethoscope

Wenzhou Bokang Instruments Co.,LtdClass IEU EUDAMEDTrade name: Teqler
VerifiedEUDAMED · official EU database
Device classification
Risk class
Class I
CND nomenclatures code
C9005
Trade name
Teqler
Implantable
No
Reusable
No
Measuring function
No
Registration information
Primary DI
06931038631031
Basic UDI
69310386STE0001LZ
Active status
No
Manufacturer
Manufacturer name
Wenzhou Bokang Instruments Co.,Ltd
Country
China
Country type
NON_EU
Address
NO.1500 NO.1500 HAINING ROAD HAIBIN LONGWAN WENZHOU
Email
bokang@bokang.com
Authorized representative
Name
Shanghai International Holding Corp. GmbH(Europe)
SRN
DE-AR-000000001
Country
Germany
Address
80 Eiffestraße Hamburg
Email
shholding@hotmail.com
Telephone
+49 40 2513175
Regulatory information
Competent authority
DE/CA05 - Behorde fur Justiz und Verbraucherschutz
Applicable legislation
MDR (REGULATION (EU) 2017/745 on medical devices)
Placed on the market
Germany
Device characteristics
Human tissues
No
Animal tissues
No
Device description (EMDN)

PHONENDOSCOPES AND STETHOSCOPES

About this record

Access comprehensive regulatory information for stethoscope 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 06931038631031 and manufactured by Wenzhou Bokang Instruments Co.,Ltd in China.

This page provides complete registration details including trade name (Teqler), manufacturer information, authorized representative details, competent authority (DE/CA05 - Behorde fur Justiz und Verbraucherschutz), 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.