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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 104070. The device is manufactured by International Biophysics Corporation, Inc. from United States, classified as General Medical Device. The authorized representative in the UK is QNET Ltd.

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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General Medical Device
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Aorta punch, single-use
MHRA Device ID: 104070โ€ขRef: 104070

Device Type

General Medical Device

Devices

Aorta punch, single-use

Type

Class IIa

Date Registered

Nov 15, 2024

Last Updated

Nov 7, 2023

Manufacturer Information

Address

2101 East St. Elmo Road, Suite 275

Austin, United States

Created Date

Sep 14, 2021

Authorized Representative

Relationship Type

UK Responsible Person

Address

Livingstone House 309 Harrow Road

Wembley, Middlesex, England, United Kingdom

Postcode: HA9 6BD

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