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 120972. The device is manufactured by Stryker Endoscopy, a division of Stryker Corporation from United States, classified as General Medical Device. The authorized representative in the UK is Stryker UK Ltd.

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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Bone curette, reusable

MHRA Device ID: 120972•Ref: 120972

Device Type

General Medical Device

Devices

Bone curette, reusable

Type

Class I

Date Registered

Nov 26, 2024

Last Updated

Dec 21, 2023

Manufacturer Information

Name

Stryker Endoscopy, a division of Stryker Corporation

Address

5900 Optical Ct

San Jose, United States

Created Date

Mar 17, 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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Other Products from Stryker Endoscopy, a division of Stryker Corporation (10)

Other Products from Same Authorized Representative (10)

Bone curette, reusable - UK MHRA Medical Device Registration

Device Type

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Type

Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

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