Inspiratory line humidification chamber, single-use - UK MHRA Medical Device Registration

Inspiratory line humidification chamber, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 184160. The device is manufactured by TELESAIR Inc from United States, classified as General Medical Device. The authorized representative in the UK is Obelis UK Ltd.

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Inspiratory line humidification chamber, single-use

MHRA Device ID: 184160•Ref: 184160

Device Type

General Medical Device

Devices

Inspiratory line humidification chamber, single-use

Type

Class IIa

Date Registered

Apr 11, 2024

Last Updated

Jan 23, 2024

Manufacturer Information

Name

TELESAIR Inc

Address

199 Technology Drive Suite 110

Irvine, California, United States

Created Date

Jan 4, 2024

Authorized Representative

Name

Obelis UK Ltd

Relationship Type

UK Responsible Person

Address

Sandford Gate, East Point Business Park

Oxford , England, United Kingdom

Postcode: OX4 6LB

DJ Fang

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Other Products from TELESAIR Inc (1)

Professional high-flow respiratory unit, humidifying

Type: General Medical Device

Registered: Apr 11, 2024

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Inspiratory line humidification chamber, single-use - UK MHRA Medical Device Registration

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