Pure Global

Vascular guide-catheter, single-use - UK MHRA Medical Device Registration

Vascular guide-catheter, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 200157. 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.

Free Database
Powered by Pure Global AI
MHRA Registered
General Medical Device
๐Ÿ‡ฌ๐Ÿ‡ง
Vascular guide-catheter, single-use
MHRA Device ID: 200157โ€ขRef: 200157

Device Type

General Medical Device

Devices

Vascular guide-catheter, single-use

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

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing