PEEP valve, single-use - UK MHRA Medical Device Registration

PEEP valve, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 185820. The device is manufactured by Dimar S.P.A from Italy, classified as General Medical Device. The authorized representative in the UK is HMC Medical UK Limited.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, device classification, authorized representative details, and related products. Pure Global AI offers free access to 150,962+ UK MHRA medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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PEEP valve, single-use

MHRA Device ID: 185820•Ref: 185820

Device Type

General Medical Device

Devices

PEEP valve, single-use

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Nov 15, 2024

Manufacturer Information

Name

Dimar S.P.A

Address

6 Via Galileo Galilei Medolla

MO, Emilia-Romagna, Italy

Created Date

Feb 2, 2024

Authorized Representative

Name

HMC Medical UK Limited

Relationship Type

UK Responsible Person

Address

Units 2 - 4 Rivington View Business park Station Road Blackrod

Bolton, England, United Kingdom

Postcode: BL65BN

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Other Products from Dimar S.P.A (10)

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PEEP valve, single-use - UK MHRA Medical Device Registration

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Date Registered

Last Updated

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DJ Fang

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