Gastro-urological guidewire, single-use - UK MHRA Medical Device Registration

Gastro-urological guidewire, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 86112. The device is manufactured by Maquet Critical Care AB from Sweden, classified as General Medical Device. The authorized representative in the UK is Getinge 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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Gastro-urological guidewire, single-use

MHRA Device ID: 86112•Ref: 86112

Device Type

General Medical Device

Devices

Gastro-urological guidewire, single-use

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Jul 24, 2024

Manufacturer Information

Name

Maquet Critical Care AB

Address

Röntgenvägen 2, SE-171 54

Solna, Sweden

Created Date

Jun 16, 2021

Authorized Representative

Name

Getinge Limited

Relationship Type

UK Responsible Person

Address

Unit 3 St Modwen Park Andressey Way Chaddesden

Derby, England, United Kingdom

Postcode: DE21 6YH

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Other Products from Maquet Critical Care AB (10)

Other Products from Same Authorized Representative (10)

Gastro-urological 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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