United Kingdom MHRA device registration 109784

Vitreous/aqueous humour replacement medium, intraoperative

United Kingdom·System or Procedure Pack·SIFI S.p.A.·Registered Apr 11, 2024

Registration details

Device ID: 109784
MHRA Reference Number: 109784
Date Registered: Apr 11, 2024
Last Updated: Jan 17, 2024

Device classification

Device Type: System or Procedure Pack
Devices: Vitreous/aqueous humour replacement medium, intraoperative
Type: System or Procedure Pack

Manufacturer

Name: SIFI S.p.A.
Address: Via Ercole Patti, 36
Aci S. Antonio, Catania, Italy
Created Date: Apr 20, 2021

Authorized Representative

Name: Qserve Group UK, Ltd.
Relationship Type: UK Responsible Person
Address: 49 Greek Street
London, England, United Kingdom
Postcode: W1D 4EG

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About this record

Vitreous/aqueous humour replacement medium, intraoperative is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 109784. The device is manufactured by SIFI S.p.A. from Italy, classified as System or Procedure Pack. The authorized representative in the UK is Qserve Group UK, Ltd. .

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