Shoulder/elbow/wrist/hand orthosis - UK MHRA Medical Device Registration

Shoulder/elbow/wrist/hand orthosis is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 129571. The device is manufactured by OPPO Medical Inc. from United States, classified as General Medical Device. The authorized representative in the UK is MT Promedt Consulting Ltd.

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Shoulder/elbow/wrist/hand orthosis

MHRA Device ID: 129571•Ref: 129571

Device Type

General Medical Device

Devices

Shoulder/elbow/wrist/hand orthosis

Type

Class I

Date Registered

Nov 26, 2024

Last Updated

Oct 25, 2024

Manufacturer Information

Name

OPPO Medical Inc.

Address

Seattle City Centre, 1420 Fifth Ave., Ste. 220080

Seattle, Washington, United States

Created Date

Dec 30, 2021

Authorized Representative

Name

MT Promedt Consulting Ltd

Relationship Type

UK Responsible Person

Address

Beaver House, 23-38 Hythe Bridge Street

Oxford, England, United Kingdom

Postcode: OX1 2EP

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Shoulder/elbow/wrist/hand orthosis - 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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