Pure Global

Laminar Flow Cabinet - EUDAMED Registration 06974738682019

Access comprehensive regulatory information for Laminar Flow Cabinet 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 06974738682019 and manufactured by Jinan Biobase Biotech Co., Ltd. in China.

This page provides complete registration details including trade name (Laminar Flow Cabinet), 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.

Free Database
Powered by Pure Global AI
EUDAMED Official Data
Class I
06974738682019
Yes
Laminar Flow Cabinet
Trade Name: Laminar Flow Cabinet
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Device Description (EMDN)

LAMINAR AIRFLOW HOODS

Device Classification
Risk Class
Class I
CND Nomenclatures Code
W02070303
Trade Name
Laminar Flow Cabinet
Implantable
No
Reusable
No
Measuring Function
No
Registration Information
Primary DI
06974738682019
Basic UDI
697473868XBX004XV
Active Status
Yes
Manufacturer
Country
China
Country Type
NON_EU
Address
OLABO Intelligent Manufacturing Industrial Park, Ancheng Town, Pingyin Country Jinan
Email
rd1@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