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 104876. The device is manufactured by Wexler Surgical Inc from United States, classified as General Medical Device. The authorized representative in the UK is UKCApartner4U Limited.

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Aorta punch, single-use

MHRA Device ID: 104876•Ref: 104876

Device Type

General Medical Device

Devices

Aorta punch, single-use

Type

Class I

Date Registered

Nov 26, 2024

Last Updated

Nov 19, 2024

Manufacturer Information

Name

Wexler Surgical Inc

Address

11333 Chimney Rock Road Suite 110

Houston, Texas, United States

Created Date

Sep 17, 2021

Authorized Representative

Name

UKCApartner4U Limited

Relationship Type

UK Responsible Person

Address

7 CAMPION WAY

BINGHAM, NOTTINGHAM, England, United Kingdom

Postcode: NG13 8 TR

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

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Date Registered

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Created Date

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