Bone nail guidewire, reusable - UK MHRA Medical Device Registration

Bone nail guidewire, reusable is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 171398. The device is manufactured by Swemac Innovation AB from Sweden, classified as General Medical Device. The authorized representative in the UK is Emergo Consulting (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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Bone nail guidewire, reusable

MHRA Device ID: 171398•Ref: 171398

Device Type

General Medical Device

Devices

Bone nail guidewire, reusable

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Apr 17, 2024

Manufacturer Information

Name

Swemac Innovation AB

Address

Cobolgatan 1

Linköping, Sweden

Created Date

Jan 7, 2022

Authorized Representative

Name

Emergo Consulting (UK) Limited

Relationship Type

UK Responsible Person

Address

Compass House, Vision Park Histon c/o Cr360 – UL International

Cambridge, England, United Kingdom

Postcode: CB24 9BZ

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Other Products from Swemac Innovation AB (10)

Other Products from Same Authorized Representative (10)

Bone nail guidewire, reusable - 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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