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Peripheral artery stent, bare-metal - UK MHRA Medical Device Registration

Peripheral artery stent, bare-metal is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 200156. The device is manufactured by Reflow Medical, Inc. from United States, classified as General Medical Device. The authorized representative in the UK is Medes 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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MHRA Registered
General Medical Device
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Peripheral artery stent, bare-metal
MHRA Device ID: 200156•Ref: 200156

Device Type

General Medical Device

Devices

Peripheral artery stent, bare-metal

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Sep 7, 2024

Manufacturer Information

Address

208 Avenida Fabricante, Suite 100

San Clemente,, California, United States

Created Date

Sep 4, 2024

Authorized Representative

Relationship Type

UK Responsible Person

Address

5 Beaumont Gate, Shenley Hil

Radlett, Herts, England, United Kingdom

Postcode: WD77AR

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