United Kingdom MHRA device registration 130101

Fructose/lactose intolerance IVD, kit, nucleic acid technique (NAT)

United Kingdom·In Vitro Diagnostic Device·Dynamic Code AB·Registered Nov 26, 2024

Registration details

Device ID: 130101
MHRA Reference Number: 130101
Date Registered: Nov 26, 2024
Last Updated: Nov 6, 2024

Device classification

Device Type: In Vitro Diagnostic Device
Devices: Fructose/lactose intolerance IVD, kit, nucleic acid technique (NAT)
Type: IVD General

Manufacturer

Name: Dynamic Code AB
Address: Fridtunagatan 24
Linköping, Östergötland, Sweden
Created Date: Dec 31, 2021

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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About this record

Fructose/lactose intolerance IVD, kit, nucleic acid technique (NAT) is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 130101. The device is manufactured by Dynamic Code AB from Sweden, classified as In Vitro Diagnostic 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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