Endoscopic-access dilator, single-use - UK MHRA Medical Device Registration

Endoscopic-access dilator, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 91838. The device is manufactured by Gyrus ACMI, Inc. from United States, classified as General Medical Device. The authorized representative in the UK is KeyMed (Medical & Industrial Equipment) Ltd..

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Endoscopic-access dilator, single-use

MHRA Device ID: 91838•Ref: 91838

Device Type

General Medical Device

Devices

Endoscopic-access dilator, single-use

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Oct 10, 2024

Manufacturer Information

Name

Gyrus ACMI, Inc.

Address

9600 Louisiana Ave.

North Brooklyn Park, United States

Created Date

Jul 23, 2021

Authorized Representative

Name

KeyMed (Medical & Industrial Equipment) Ltd.

Relationship Type

UK Responsible Person

Address

Keymed House Stock Road

Southend-on-sea, Essex, United Kingdom

Postcode: SS2 5QH

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Other Products from Gyrus ACMI, Inc. (10)

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Endoscopic-access dilator, single-use - UK MHRA Medical Device Registration

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Date Registered

Last Updated

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Created Date

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DJ Fang

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