FDA Registration Number: 3005533818

Last Validated: May 21, 2024

Status: Valid

Valid2024 U.S. FDA Medical Device Establishment Registration

PROSYS INTERNATIONAL LTD

Establishment Information

suite 303 Highland House
165 The Broadway
Wimbledon England, GB SW19 1NE

U.S. Agent and Official Correspondent

Registrar Corp
144 Research Drive
Hampton VA, USA 23666
Registration of a device establishment, assignment of a registration number, or listing of a medical device does not in any way denote approval of the establishment or its products by U.S. FDA.

Listings on file with FDA

Device Name Product Code Status Last Validated  
Tubes, Gastrointestinal (And Accessories) KNT Valid May 20, 2024

Device Listing

Device Name

Tubes, Gastrointestinal (And Accessories)

Product Code

KNT

Company Function(s)

Foreign Exporter, Specification Developer

Proprietary Name(s)

Avantgarde +T
Protector, Skin Pressure FMP Valid May 20, 2024

Device Listing

Device Name

Protector, Skin Pressure

Product Code

FMP

Company Function(s)

Foreign Exporter, Specification Developer

Proprietary Name(s)

Offload Bootee
Cushion, Flotation KIC Valid May 20, 2024

Device Listing

Device Name

Cushion, Flotation

Product Code

KIC

Company Function(s)

Foreign Exporter, Specification Developer

Proprietary Name(s)

Prevasse

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