Diskectomy system, percutaneous, automatic - UK MHRA Medical Device Registration

Diskectomy system, percutaneous, automatic is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 126179. The device is manufactured by Stryker Instruments, a division of Stryker Corporation from United States, classified as General Medical Device. The authorized representative in the UK is Stryker UK Ltd.

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Diskectomy system, percutaneous, automatic

MHRA Device ID: 126179•Ref: 126179

Device Type

General Medical Device

Devices

Diskectomy system, percutaneous, automatic

Type

Class IIb

Date Registered

Sep 24, 2024

Last Updated

Oct 7, 2023

Manufacturer Information

Name

Stryker Instruments, a division of Stryker Corporation

Address

4100 E. Milham Ave

Kalamazoo, Michigan, United States

Created Date

Mar 3, 2021

Authorized Representative

Name

Stryker UK Ltd

Relationship Type

UK Responsible Person

Address

Stryker House Hambridge Road

Newbury, Berkshire, England, United Kingdom

Postcode: RG14 5AW

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Diskectomy system, percutaneous, automatic - UK MHRA Medical Device Registration

Device Type

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Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

DJ Fang

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