Vascular graft extraluminal mesh-sleeve, peripheral - UK MHRA Medical Device Registration

Vascular graft extraluminal mesh-sleeve, peripheral is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 63917. The device is manufactured by Vascular Graft Solutions Ltd. from Israel, classified as General Medical Device. The authorized representative in the UK is Medimap 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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Vascular graft extraluminal mesh-sleeve, peripheral

MHRA Device ID: 63917•Ref: 63917

Device Type

General Medical Device

Devices

Vascular graft extraluminal mesh-sleeve, peripheral

Type

Class IIb

Date Registered

Nov 26, 2024

Last Updated

Mar 23, 2024

Manufacturer Information

Name

Vascular Graft Solutions Ltd.

Address

24 Raoul Wallenberg Street

Tel Aviv, Israel

Created Date

Jan 4, 2021

Authorized Representative

Name

Medimap Ltd

Relationship Type

UK Responsible Person

Address

2 The Drift

Thurston, Suffolk, United Kingdom

Postcode: IP31 3RT

DJ Fang

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Other Products from Vascular Graft Solutions Ltd. (4)

Other Products from Same Authorized Representative (10)

Vascular graft extraluminal mesh-sleeve, peripheral - 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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Wireless patient monitor/sensor reporting software, professional-only

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Vascular graft extraluminal mesh-sleeve, coronary

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