Pure Global

Fluorescent immunoassay/spectrophotometry analyser IVD, point-of-care - UK MHRA Medical Device Registration

Fluorescent immunoassay/spectrophotometry analyser IVD, point-of-care is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 111554. The device is manufactured by i-SENS, Inc. from South Korea, classified as In Vitro Diagnostic Device. The authorized representative in the UK is MT Promedt Consulting 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.

Free Database
Powered by Pure Global AI
MHRA Registered
In Vitro Diagnostic Device
๐Ÿ‡ฌ๐Ÿ‡ง
Fluorescent immunoassay/spectrophotometry analyser IVD, point-of-care
MHRA Device ID: 111554โ€ขRef: 111554

Device Type

In Vitro Diagnostic Device

Devices

Fluorescent immunoassay/spectrophotometry analyser IVD, point-of-care

Type

IVD General

Date Registered

Nov 26, 2024

Last Updated

May 9, 2024

Manufacturer Information

Address

43, Banpo-daero 28-gil, Seocho-gu

Seoul , South Korea

Created Date

Jul 21, 2021

Authorized Representative

Relationship Type

UK Responsible Person

Address

Beaver House, 23-38 Hythe Bridge Street

Oxford, England, United Kingdom

Postcode: OX1 2EP

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing