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EUDAMED registration 06932562300912Yes

Temperature Probe

Guangdong Biolight Meditech Co., LtdClass IIaEU EUDAMEDTrade name: Temperature Probe
VerifiedEUDAMED · official EU database
Device classification
Risk class
Class IIa
CND nomenclatures code
V03010201
Trade name
Temperature Probe
Implantable
No
Reusable
No
Measuring function
Yes
Registration information
Primary DI
06932562300912
Basic UDI
69325623500075H
Version date
February 08, 2025
Manufacturer last update
June 14, 2023
Active status
Yes
Manufacturer
Manufacturer name
Guangdong Biolight Meditech Co., Ltd
Country
China
Country type
NON_EU
Address
No.2 No.2 Innovation First Road, Technical Innovation Coast, Hi-tech Zone, Zhuhai, P.R. China Zhuhai
Email
hou_d@blt.com.cn
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
Market available
France:2024-09-20~2028-04-10, Germany:2024-09-20~2028-04-10, Poland:2024-09-20~2028-04-10
Device characteristics
Human tissues
No
Animal tissues
No
Device description (EMDN)

TEMPERATURE MONITORING CUTANEOUS PROBES

About this record

Access comprehensive regulatory information for Temperature Probe in the European Union medical device market through Pure Global AI's free database. This Class IIa device is registered with EU EUDAMED under Primary DI 06932562300912 and manufactured by Guangdong Biolight Meditech Co., Ltd in China.

This page provides complete registration details including trade name (Temperature Probe), 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.