Vertebral bone biopsy procedure kit, single-use - UK MHRA Medical Device Registration

Vertebral bone biopsy procedure kit, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 94625. 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.

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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Vertebral bone biopsy procedure kit, single-use

MHRA Device ID: 94625•Ref: 94625

Device Type

General Medical Device

Devices

Vertebral bone biopsy procedure kit, single-use

Type

Class IIa

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

DJ Fang

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Vertebral bone biopsy procedure kit, single-use - 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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