United Kingdom MHRA device registration 200500

Vascular catheter/cannula flush solution, non-anticoagulant, non-antimicrobial

United Kingdom·General Medical Device·PENTAFERTE ITALIA s.r.l.·Registered Nov 26, 2024

Registration details

Device ID: 200500
MHRA Reference Number: 200500
Date Registered: Nov 26, 2024
Last Updated: Oct 15, 2024

Device classification

Device Type: General Medical Device
Devices: Vascular catheter/cannula flush solution, non-anticoagulant, non-antimicrobial
Type: Class IIb

Manufacturer

Name: PENTAFERTE ITALIA s.r.l.
Address: Viale Piane Nocella, 23
CAMPLI , TE, Italy
Created Date: Nov 14, 2022

Authorized Representative

Name: Advena Ltd
Relationship Type: UK Responsible Person
Address: Pure Offices Plato Close
Warwick, England, United Kingdom
Postcode: CV34 6WE

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About this record

Vascular catheter/cannula flush solution, non-anticoagulant, non-antimicrobial is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 200500. The device is manufactured by PENTAFERTE ITALIA s.r.l. from Italy, classified as General Medical Device. The authorized representative in the UK is Advena 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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