Flexible endoscopic biopsy forceps, single-use - UK MHRA Medical Device Registration

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 195304. The device is manufactured by Scivita Medical Technology Co., Ltd. from China, classified as General Medical Device. The authorized representative in the UK is Etheria Medical 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.

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Flexible endoscopic biopsy forceps, single-use

MHRA Device ID: 195304•Ref: 195304

Device Type

General Medical Device

Devices

Flexible endoscopic biopsy forceps, single-use

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Mar 25, 2024

Manufacturer Information

Name

Scivita Medical Technology Co., Ltd.

Address

No. 2, Qingqiu Street, Suzhou Industrial Park

Suzhou, Jiangsu, China

Created Date

Apr 20, 2023

Authorized Representative

Name

Etheria Medical Ltd

Relationship Type

UK Responsible Person

Address

The Old brush Factory Unit 2D Whickham Industrial Estate, Swalwell

Newcastle Upon Tyne, United Kingdom

Postcode: NE16 3DA

DJ Fang

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Other Products from Scivita Medical Technology Co., Ltd. (9)

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Flexible endoscopic biopsy forceps, single-use - UK MHRA Medical Device Registration

Device Type

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Date Registered

Last Updated

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Created Date

Name

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Address

DJ Fang

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