Vitreous/aqueous humour replacement medium, intraoperative - UK MHRA Medical Device Registration

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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Vitreous/aqueous humour replacement medium, intraoperative

MHRA Device ID: 109784•Ref: 109784

Device Type

System or Procedure Pack

Devices

Vitreous/aqueous humour replacement medium, intraoperative

Type

System or Procedure Pack

Date Registered

Apr 11, 2024

Last Updated

Jan 17, 2024

Manufacturer Information

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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Vitreous/aqueous humour replacement medium, intraoperative - UK MHRA Medical Device Registration

Device Type

Devices

Type

Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

DJ Fang

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