Microvent
- Risk class
- Class IIa
- CND nomenclatures code
- Z12030103
- Trade name
- Microvent
- Implantable
- No
- Reusable
- No
- Measuring function
- No
- Primary DI
- 05052270201309
- Basic UDI
- B-05052270201309
- Version date
- February 20, 2023
- Manufacturer last update
- June 30, 2021
- Active status
- Yes
- Manufacturer name
- BNOS MediTECH
- Country
- United Kingdom (ex Northern Ireland)
- Country type
- NON_EU
- Address
- 9 Fifth Avenue CO9 2SZ Halstead, Essex,
- sales@meditech.uk.com
- SRN
- IE-AR-000002496
- Country
- Ireland
- Address
- Block B, The Crescent Building, Dublin 9
- EU-Rep@medicaldevicemanagement.com
- Telephone
- +353 (0) 1893 4143
- 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
- Human tissues
- No
- Animal tissues
- No
PULMONARY VENTILATORS FOR NON–HOSPITAL USE
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 05052270201309 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.