Polyethylene patella prosthesis - UK MHRA Medical Device Registration

Polyethylene patella prosthesis is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 68222. The device is manufactured by MAKO Surgical Corp 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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Polyethylene patella prosthesis

MHRA Device ID: 68222•Ref: 68222

Device Type

General Medical Device

Devices

Polyethylene patella prosthesis

Type

Class III

Date Registered

Nov 26, 2024

Last Updated

Dec 5, 2023

Manufacturer Information

Name

MAKO Surgical Corp

Address

3365 Enterprise Avenue

Weston, Florida, United States

Created Date

Mar 2, 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 MAKO Surgical Corp (10)

Other Products from Same Authorized Representative (10)

Polyethylene patella prosthesis - UK MHRA Medical Device Registration

Device Type

Devices

Type

Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

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