Neurosurgical curette, single-use - UK MHRA Medical Device Registration

Neurosurgical curette, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 109259. The device is manufactured by Medtronic Sofamor Danek Inc. from United States, classified as General Medical Device. The authorized representative in the UK is Medtronic Limited.

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Neurosurgical curette, single-use

MHRA Device ID: 109259•Ref: 109259

Device Type

General Medical Device

Devices

Neurosurgical curette, single-use

Type

Class I

Date Registered

Nov 26, 2024

Last Updated

Dec 16, 2023

Manufacturer Information

Name

Medtronic Sofamor Danek Inc.

Address

1800 Pyramid Place

Memphis, TN, United States

Created Date

Mar 9, 2021

Authorized Representative

Name

Medtronic Limited

Relationship Type

UK Responsible Person

Address

Building 9 Croxley Park

Watford, Herts, England, United Kingdom

Postcode: WD18 8WW

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Other Products from Medtronic Sofamor Danek Inc. (10)

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Neurosurgical curette, single-use - UK MHRA Medical Device Registration

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Devices

Type

Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

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