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Mandible-repositioning sleep-disordered breathing orthosis - UK MHRA Medical Device Registration

Mandible-repositioning sleep-disordered breathing orthosis is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 191784. The device is manufactured by Snoring Relief Labs, Inc. from United States, classified as General Medical Device. The authorized representative in the UK is CASUS UKRP 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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Mandible-repositioning sleep-disordered breathing orthosis
MHRA Device ID: 191784โ€ขRef: 191784

Device Type

General Medical Device

Devices

Mandible-repositioning sleep-disordered breathing orthosis

Type

Class I

Date Registered

Nov 26, 2024

Last Updated

May 4, 2024

Manufacturer Information

Address

4007 Pretense Ct

Fair Oaks, California, United States

Created Date

Apr 19, 2024

Authorized Representative

Relationship Type

UK Responsible Person

Address

107-111 Fleet Street

London, England, United Kingdom

Postcode: EC4A 2AB

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