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 99091. The device is manufactured by Applied Medical Technology, Inc. from United States, classified as General Medical Device. The authorized representative in the UK is MDSS-UK RP 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: 99091•Ref: 99091

Device Type

General Medical Device

Devices

Gastro-urological guidewire, single-use

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Jan 23, 2024

Manufacturer Information

Name

Applied Medical Technology, Inc.

Address

8006 Katherine Blvd.

Brecksville, OH, United States

Created Date

Apr 8, 2021

Authorized Representative

Name

MDSS-UK RP LIMITED

Relationship Type

UK Responsible Person

Address

6 Wilmslow Road, Rusholme

Manchester, England, United Kingdom

Postcode: M14 5TP

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Other Products from Applied Medical Technology, Inc. (10)

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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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