Orthopaedic guidewire, single-use - UK MHRA Medical Device Registration

Orthopaedic guidewire, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 195416. The device is manufactured by Orthopediatrics Canada ULC, d.b.a. Pega Medical Inc. from Canada, classified as General Medical Device. The authorized representative in the UK is MedEnvoy UK 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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Orthopaedic guidewire, single-use

MHRA Device ID: 195416•Ref: 195416

Device Type

General Medical Device

Devices

Orthopaedic guidewire, single-use

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Jun 22, 2024

Manufacturer Information

Name

Orthopediatrics Canada ULC, d.b.a. Pega Medical Inc.

Address

1111 Autoroute Chomedey

Laval, Canada

Created Date

Jun 18, 2024

Authorized Representative

Name

MedEnvoy UK Limited

Relationship Type

UK Responsible Person

Address

85 Great Portland Street First Floor

London, England, United Kingdom

Postcode: W1W 7LT

DJ Fang

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Other Products from Orthopediatrics Canada ULC, d.b.a. Pega Medical Inc. (10)

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Orthopaedic guidewire, 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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