United Kingdom MHRA device registration 181052

Electric infusion pump administration set, single-use

United Kingdom flagUnited Kingdom·General Medical Device·Medica S.p.A. ·Registered Nov 26, 2024
Registration details
Device ID
181052
MHRA Reference Number
181052
Date Registered
Nov 26, 2024
Last Updated
Oct 24, 2024
Device classification
Device Type
General Medical Device
Devices
Electric infusion pump administration set, single-use
Type
Class IIa
Manufacturer
Address
Via degli Artigiani 7
Medolla, Italy
Created Date
Oct 31, 2023
Authorized Representative
Relationship Type
UK Responsible Person
Address
85 Great Portland Street First Floor
London, England, United Kingdom
Postcode: W1W 7LT
Similar products

Devices with a matching generic name or device type registered with MHRA

Other products from Medica S.p.A.

Additional devices registered by the same manufacturer

Other products from same authorized representative

Additional devices represented by MedEnvoy UK Limited in the UK

Liposuction system
Type: General Medical Device
Manufacturer: Honeywell Healthcare Solutions GmbH
Device ID: 176919
C-reactive protein (CRP) IVD, kit, enzyme immunoassay (EIA)Nov 26, 2024
Type: In Vitro Diagnostic Device
Manufacturer: Diagnostics Biochem Canada, Inc.
Device ID: 202174
Reverse triiodothyronine (reverse T3) IVD, kit, enzyme immunoassay (EIA)Nov 26, 2024
Type: In Vitro Diagnostic Device
Manufacturer: Diagnostics Biochem Canada, Inc.
Device ID: 202198
Free estriol (oestriol) IVD, kit, enzyme immunoassay (EIA)Nov 26, 2024
Type: In Vitro Diagnostic Device
Manufacturer: Diagnostics Biochem Canada, Inc.
Device ID: 202185
Free thyroxine (FT4) IVD, kit, enzyme immunoassay (EIA)Nov 26, 2024
Type: In Vitro Diagnostic Device
Manufacturer: Diagnostics Biochem Canada, Inc.
Device ID: 202187
Renin IVD, kit, enzyme immunoassay (EIA)Nov 26, 2024
Type: In Vitro Diagnostic Device
Manufacturer: Diagnostics Biochem Canada, Inc.
Device ID: 202193
Estrone (oestrone) IVD, kit, enzyme immunoassay (EIA)Nov 26, 2024
Type: In Vitro Diagnostic Device
Manufacturer: Diagnostics Biochem Canada, Inc.
Device ID: 202182
Thyroid stimulating hormone (TSH) IVD, kit, enzyme immunoassay (EIA)Nov 26, 2024
Type: In Vitro Diagnostic Device
Manufacturer: Diagnostics Biochem Canada, Inc.
Device ID: 202201
Total cortisol IVD, kit, enzyme immunoassay (EIA)Nov 26, 2024
Type: In Vitro Diagnostic Device
Manufacturer: Diagnostics Biochem Canada, Inc.
Device ID: 202176
C-peptide IVD, kit, enzyme immunoassay (EIA)Nov 26, 2024
Type: In Vitro Diagnostic Device
Manufacturer: Diagnostics Biochem Canada, Inc.
Device ID: 202173
About this record

Electric infusion pump administration set, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 181052. The device is manufactured by Medica S.p.A. from Italy, classified as General Medical Device. The authorized representative in the UK is MedEnvoy UK Limited.

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 DatabasePowered by Pure Global AIMHRA RegisteredGeneral Medical Device