Aorta punch, single-use - UK MHRA Medical Device Registration

Aorta punch, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 75955. The device is manufactured by A&E Medical Corporation from United States, classified as General Medical Device. The authorized representative in the UK is Zimmer Biomet 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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Aorta punch, single-use

MHRA Device ID: 75955•Ref: 75955

Device Type

General Medical Device

Devices

Aorta punch, single-use

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Apr 23, 2024

Manufacturer Information

Name

A&E Medical Corporation

Address

A&E Medical Corporation 5206 Asbury Road PO Box 758

Farmingdale , New Jersey , United States

Created Date

Apr 26, 2021

Authorized Representative

Name

Zimmer Biomet UK Limited

Relationship Type

UK Responsible Person

Address

Stella Building Windmill Hill Business Park Whitehill Way

Swindon, England, United Kingdom

Postcode: SN5 6NX

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Other Products from A&E Medical Corporation (5)

Other Products from Same Authorized Representative (10)

Aorta punch, 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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