Uterine tenaculum - UK MHRA Medical Device Registration

Uterine tenaculum is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 180135. The device is manufactured by ASPIVIX SA from Switzerland, classified as General Medical Device. The authorized representative in the UK is Obelis UK 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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Uterine tenaculum

MHRA Device ID: 180135•Ref: 180135

Device Type

General Medical Device

Devices

Uterine tenaculum

Type

Class I

Date Registered

Nov 26, 2024

Last Updated

Jul 23, 2024

Manufacturer Information

Name

ASPIVIX SA

Address

Rue de la Corniche 8

Epalinges, Switzerland, Switzerland

Created Date

Oct 10, 2023

Authorized Representative

Name

Obelis UK Ltd

Relationship Type

UK Responsible Person

Address

Sandford Gate, East Point Business Park

Oxford , England, United Kingdom

Postcode: OX4 6LB

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Uterine tenaculum - UK MHRA Medical Device Registration

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