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Swab - EUDAMED Registration 06974901971070

Access comprehensive regulatory information for Swab 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 06974901971070 and manufactured by Shandong Bohong Gene Technology Co., Ltd. in China.

This page provides complete registration details including trade name (Swab), 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
06974901971070
No
Swab
Trade Name: Swab
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Device Description (EMDN)

SAMPLES COLLECTION DEVICES - OTHER

Device Classification
Risk Class
Class I
CND Nomenclatures Code
W05019099
Trade Name
Swab
Implantable
No
Reusable
No
Measuring Function
No
Registration Information
Primary DI
06974901971070
Basic UDI
6974901BH007UA
Version Date
November 11, 2022
Manufacturer Last Update
July 12, 2022
Active Status
No
Manufacturer
Country
China
Country Type
NON_EU
Address
1st Floor of Building 2, BIOBASE Headquarters, north of Gangyuan 7th Road and west of Gangxingyuan Road, Pilot Free Trade Zone of Jinan 250101 Jinan
Email
base@biobase.cn
Authorized Representative
SRN
DE-AR-000005110
Country
Germany
Address
1 Kochstr Willich
Email
info.m@luxuslw.de
Telephone
+49 1715605732
Regulatory Information
Competent Authority
DE/CA20, Bezirksregierung Düsseldorf Dezernat 24
Applicable Legislation
MDR (REGULATION (EU) 2017/745 on medical devices)
Placed On The Market
Germany
Device Characteristics
Human Tissues
No
Animal Tissues
No