Arteriovenous fistula extraluminal mesh-sleeve - UK MHRA Medical Device Registration

Arteriovenous fistula extraluminal mesh-sleeve is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 85674. The device is manufactured by Laminate Medical Technologies 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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Arteriovenous fistula extraluminal mesh-sleeve

MHRA Device ID: 85674•Ref: 85674

Device Type

General Medical Device

Devices

Arteriovenous fistula extraluminal mesh-sleeve

Type

Class IIb

Date Registered

Nov 26, 2024

Last Updated

May 18, 2024

Manufacturer Information

Name

Laminate Medical Technologies Ltd

Address

24 Raoul Wallenberg Street

Tel Aviv, Israel

Created Date

Jun 16, 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 Laminate Medical Technologies Ltd (1)

Open-surgery blood vessel sizer, single-use

Type: General Medical Device

Registered: Nov 26, 2024

Other Products from Same Authorized Representative (10)

Arteriovenous fistula extraluminal mesh-sleeve - UK MHRA Medical Device Registration

Device Type

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Type

Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

DJ Fang

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