United Kingdom MHRA device registration 199050
Flexible endoscopic biopsy forceps, single-use
United Kingdom·General Medical Device·Hangzhou AGS MedTech Co., Ltd.·Registered Nov 26, 2024Registration details
- Device ID
- 199050
- MHRA Reference Number
- 199050
- Date Registered
- Nov 26, 2024
- Last Updated
- Aug 15, 2024
Device classification
- Device Type
- General Medical Device
- Devices
- Flexible endoscopic biopsy forceps, single-use
- Type
- Class IIa
Manufacturer
- Address
- Building 2, 5 and 7, No.389 Xingzhong Road, Linping District Hangzhou, Zhejiang, China
- Created Date
- May 7, 2021
Authorized Representative
- Relationship Type
- UK Responsible Person
- Address
- 19 MEZZANINE FLOOR 19-21 CRAWFORD STREET London, England, United KingdomPostcode: W1H 1PJ
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About this record
Flexible endoscopic biopsy forceps, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 199050. The device is manufactured by Hangzhou AGS MedTech Co., Ltd. from China, classified as General Medical Device. The authorized representative in the UK is KINGSMEAD SERVICE LIMITED.
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