Coronary angioplasty balloon catheter, basic
United Kingdom·General Medical Device·Goodman Co., Ltd.·Registered Nov 26, 2024- Device ID
- 203412
- MHRA Reference Number
- 203412
- Date Registered
- Nov 26, 2024
- Last Updated
- Apr 23, 2024
- Device Type
- General Medical Device
- Devices
- Coronary angioplasty balloon catheter, basic
- Type
- Class III
- Address
- 5F KDX Nagoya Sakae Building, 4-5-3 Sakae Naka-ku Nagoya,, Aichi, Japan
- Created Date
- Feb 10, 2022
- Relationship Type
- UK Responsible Person
- Address
- Compass House, Vision Park Histon c/o Cr360 – UL International Cambridge, England, United KingdomPostcode: CB24 9BZ
Devices with a matching generic name or device type registered with MHRA
Additional devices registered by the same manufacturer
Additional devices represented by Emergo Consulting (UK) Limited in the UK
Coronary angioplasty balloon catheter, basic is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 203412. The device is manufactured by Goodman Co., Ltd. from Japan, classified as General Medical Device. The authorized representative in the UK is Emergo Consulting (UK) Limited .
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.