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SPECIMEN BAG - EUDAMED Registration 06977995690025

Access comprehensive regulatory information for SPECIMEN BAG in the European Union medical device market through Pure Global AI's free database. This Class A device is registered with EU EUDAMED under Primary DI 06977995690025 and manufactured by HENG RONG (XIAMEN) PLASTIC PRODUCTS CO., LTD. in China.

This page provides complete registration details including trade name (Specimen bag), manufacturer information, authorized representative details, competent authority (The Medicines and Healthcare Products Regulatory Agency), 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 A
06977995690025
No
SPECIMEN BAG
Trade Name: Specimen bag
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Device Description (EMDN)

SAMPLES TRANSPORT, BAGS

Device Classification
Risk Class
Class A
CND Nomenclatures Code
W05020105
Trade Name
Specimen bag
Implantable
No
Reusable
No
Measuring Function
No
Registration Information
Primary DI
06977995690025
Basic UDI
697799569LABSZB001HH
Active Status
No
Manufacturer
Country
China
Country Type
NON_EU
Address
No.3 XiangHong Rd., XiangAn District Xiamen City, Fujian Province
Email
hui@hr-plastic.com
Authorized Representative
SRN
XI-AR-000001836
Country
United Kingdom (Northern Ireland only)
Address
Enterprise Hub, NW Business Complex, Derry
Email
AuthRep@CE-marking.eu
Telephone
+44(33)33031126
Regulatory Information
Competent Authority
The Medicines and Healthcare Products Regulatory Agency
Applicable Legislation
IVDR (REGULATION (EU) 2017/746 on in vitro diagnostic medical devices)
Placed On The Market
Spain
Device Characteristics
Human Tissues
No
Animal Tissues
No