Bone curette, reusable - UK MHRA Medical Device Registration

Bone curette, reusable is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 189323. The device is manufactured by Smith & Nephew, Inc., Endoscopy Division from United States, classified as General Medical Device. The authorized representative in the UK is T.J.Smith and Nephew,Limited.

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Bone curette, reusable

MHRA Device ID: 189323•Ref: 189323

Device Type

General Medical Device

Devices

Bone curette, reusable

Type

Class I

Date Registered

Nov 26, 2024

Last Updated

Jan 20, 2024

Manufacturer Information

Name

Smith & Nephew, Inc., Endoscopy Division

Address

150 Minuteman Road

Andover, Massachusetts, United States

Created Date

Mar 5, 2021

Authorized Representative

Name

T.J.Smith and Nephew,Limited

Relationship Type

UK Responsible Person

Address

101 Hessle Road

Hull, England, United Kingdom

Postcode: HU3 2BN

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Bone curette, reusable - UK MHRA Medical Device Registration

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