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Microvent - EUDAMED Registration 05052270201408

Access comprehensive regulatory information for Microvent 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 05052270201408 and manufactured by BNOS MediTECH in United Kingdom (ex Northern Ireland).

This page provides complete registration details including trade name (Microvent ), manufacturer information, authorized representative details, competent authority (Health Products Regulatory Authority, Medical Devices Department), 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 IIa
05052270201408
Yes
Microvent
Trade Name: Microvent
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Device Description (EMDN)

PULMONARY VENTILATORS FOR NONโ€“HOSPITAL USE

Device Classification
Risk Class
Class IIa
CND Nomenclatures Code
Z12030103
Trade Name
Microvent
Implantable
No
Reusable
No
Measuring Function
No
Registration Information
Primary DI
05052270201408
Basic UDI
B-05052270201408
Version Date
February 20, 2023
Manufacturer Last Update
June 30, 2021
Active Status
Yes
Manufacturer
Manufacturer Name
BNOS MediTECH
Country
United Kingdom (ex Northern Ireland)
Country Type
NON_EU
Address
9 Fifth Avenue CO9 2SZ Halstead, Essex,
Email
sales@meditech.uk.com
Authorized Representative
SRN
IE-AR-000002496
Country
Ireland
Address
Block B, The Crescent Building, Dublin 9
Email
EU-Rep@medicaldevicemanagement.com
Telephone
+353 (0) 1893 4143
Regulatory Information
Competent Authority
Health Products Regulatory Authority, Medical Devices Department
Applicable Legislation
MDD (Directive 93/42/EEC on Medical Devices)
Placed On The Market
Netherlands
Market Available
Italy:2022-09-01~None, Netherlands:2004-06-01~None, Poland:2018-01-01~None
Device Characteristics
Human Tissues
No
Animal Tissues
No