Cardiac/peripheral vascular guidewire, single-use
United Kingdom·General Medical Device·EPflex Feinwerktechnik GmbH·Registered Nov 26, 2024- Device ID
- 91265
- MHRA Reference Number
- 91265
- Date Registered
- Nov 26, 2024
- Last Updated
- Jun 6, 2024
- Device Type
- General Medical Device
- Devices
- Cardiac/peripheral vascular guidewire, single-use
- Type
- Class IIa
- Address
- Im Schwöllbogen 24 Dettingen an der Erms , Germany
- Created Date
- Jul 30, 2021
- Relationship Type
- UK Responsible Person
- Address
- 2 St Andrews Place Lewes, East Sussex, England, United KingdomPostcode: BN7 1UP
Devices with a matching generic name or device type registered with MHRA
Additional devices registered by the same manufacturer
Additional devices represented by MEDAGENT INTERNATIONAL UK LIMITED in the UK
Cardiac/peripheral vascular guidewire, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 91265. The device is manufactured by EPflex Feinwerktechnik GmbH from Germany, classified as General Medical Device. The authorized representative in the UK is MEDAGENT INTERNATIONAL 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.