General surgical procedure kit, non-medicated, single-use - UK MHRA Medical Device Registration

General surgical procedure kit, non-medicated, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 90450. The device is manufactured by BETATEX S.p.a from Italy, classified as General Medical Device. The authorized representative in the UK is Advena 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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General surgical procedure kit, non-medicated, single-use

MHRA Device ID: 90450•Ref: 90450

Device Type

General Medical Device

Devices

General surgical procedure kit, non-medicated, single-use

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Nov 8, 2024

Manufacturer Information

Name

BETATEX S.p.a

Address

VIA RAFFAELLO 2

ASSISI , Perugia, Italy

Created Date

Jun 28, 2021

Authorized Representative

Name

Advena Ltd

Relationship Type

UK Responsible Person

Address

Pure Offices Plato Close

Warwick, England, United Kingdom

Postcode: CV34 6WE

DJ Fang

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Other Products from BETATEX S.p.a (2)

Patient surgical drape, single-use

Type: General Medical Device

Registered: Nov 26, 2024

Ophthalmic surgical drape

Type: General Medical Device

Registered: Nov 26, 2024

Other Products from Same Authorized Representative (10)

General surgical procedure kit, non-medicated, single-use - UK MHRA Medical Device Registration

Device Type

Devices

Type

Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

DJ Fang

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