Anaesthesia face mask, single-use - UK MHRA Medical Device Registration

Anaesthesia face mask, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 99030. The device is manufactured by Respironics Inc from United States, classified as General Medical Device. The authorized representative in the UK is Philips Electronics UK Ltd.

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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Anaesthesia face mask, single-use

MHRA Device ID: 99030•Ref: 99030

Device Type

General Medical Device

Devices

Anaesthesia face mask, single-use

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Jul 16, 2024

Manufacturer Information

Name

Respironics Inc

Address

1001 Murry Ridge Lane

Murrysville, United States

Created Date

Aug 25, 2021

Authorized Representative

Name

Philips Electronics UK Ltd

Relationship Type

UK Responsible Person

Address

Ascent 1 Farnborough Aerospace Centre

Farnborough, Hampshire, England, United Kingdom

Postcode: GU14 6XW

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Other Products from Respironics Inc (10)

Other Products from Same Authorized Representative (10)

Anaesthesia face mask, single-use - UK MHRA Medical Device Registration

Device Type

Devices

Type

Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

DJ Fang

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