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Transobturator needle, single-use - UK MHRA Medical Device Registration

Transobturator needle, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 162106. The device is manufactured by DESARROLLO E INVESTIGACIÓN MÉDICA ARAGONESA S.L. (DIMA S.L.) from Spain, classified as General Medical Device. The authorized representative in the UK is AF PHARMA SERVICE 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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General Medical Device
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Transobturator needle, single-use
MHRA Device ID: 162106•Ref: 162106

Device Type

General Medical Device

Devices

Transobturator needle, single-use

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Nov 15, 2023

Manufacturer Information

Address

Polígono Industrial Mediavega, parcela 2.8

Calatayud , Zaragoza, Spain

Created Date

Dec 1, 2022

Authorized Representative

Relationship Type

UK Responsible Person

Address

Suite 140 Temple Chambers 3-7 Temple Avenue

London, England, United Kingdom

Postcode: EC4Y 0DA

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