Pure Global

Coronary angioplasty balloon catheter, cutting/scoring - UK MHRA Medical Device Registration

Coronary angioplasty balloon catheter, cutting/scoring is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 152749. The device is manufactured by Philips Image Guided Therapy Corporation from United States, classified as General Medical Device. The authorized representative in the UK is Philips Electronics UK 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
Coronary angioplasty balloon catheter, cutting/scoring
MHRA Device ID: 152749โ€ขRef: 152749

Device Type

General Medical Device

Devices

Coronary angioplasty balloon catheter, cutting/scoring

Type

Class III

Date Registered

Nov 26, 2024

Last Updated

Nov 16, 2024

Manufacturer Information

Address

9965 Federal Drive

Colorado Springs, United States

Created Date

Feb 7, 2022

Authorized Representative

Relationship Type

UK Responsible Person

Address

Ascent 1 Farnborough Aerospace Centre

Farnborough, Hampshire, England, United Kingdom

Postcode: GU14 6XW

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing