Pure Global

Sm/RNP antibody IVD, kit, enzyme immunoassay (EIA) - UK MHRA Medical Device Registration

Sm/RNP antibody IVD, kit, enzyme immunoassay (EIA) is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 112047. The device is manufactured by ORGENTEC Diagnostika GmbH from Germany, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Qarad 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.

Free Database
Powered by Pure Global AI
MHRA Registered
In Vitro Diagnostic Device
๐Ÿ‡ฌ๐Ÿ‡ง
Sm/RNP antibody IVD, kit, enzyme immunoassay (EIA)
MHRA Device ID: 112047โ€ขRef: 112047

Device Type

In Vitro Diagnostic Device

Devices

Sm/RNP antibody IVD, kit, enzyme immunoassay (EIA)

Type

IVD General

Date Registered

Nov 26, 2024

Last Updated

Jun 15, 2024

Manufacturer Information

Address

Carl-Zeiss-Str. 49-51

Mainz, Rheinhessen-Pfalz, Germany

Created Date

Aug 10, 2021

Authorized Representative

Relationship Type

UK Responsible Person

Address

8 Northumberland Ave

Westminster, London , England, United Kingdom

Postcode: WC2N 5BY

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing