Endoscopic-access dilator, single-use
- Device ID
- 189081
- MHRA Reference Number
- 189081
- Date Registered
- Nov 26, 2024
- Last Updated
- Apr 12, 2024
- Device Type
- General Medical Device
- Devices
- Endoscopic-access dilator, single-use
- Type
- Class I
- Name
- Teleflex Medical
- Address
- IDA Business and Technology Park Dublin Road Athlone, Co. Westmeath, Ireland
- Created Date
- Apr 19, 2021
- Name
- TFX Group Ltd
- Relationship Type
- UK Responsible Person
- Address
- Grosvenor House Horseshoe Crescent Old Town Beaconsfield, England, United KingdomPostcode: HP9 1LJ
Devices with a matching generic name or device type registered with MHRA
Additional devices registered by the same manufacturer
Additional devices represented by TFX Group Ltd in the UK
Endoscopic-access dilator, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 189081. The device is manufactured by Teleflex Medical from Ireland, classified as General Medical Device. The authorized representative in the UK is TFX Group 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.