FDA Registration Number: 3005533818

Last Validated: March 19, 2025

Status: Valid

Valid2025 U.S. FDA Medical Device Establishment Registration

PROSYS INTERNATIONAL LTD

Establishment Information

Suite 4
2 Allington Close; Wimbledon; England
London London, City of, GB SW19 5AP

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 March 18, 2025

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 March 18, 2025

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 March 18, 2025

Device Listing

Device Name

Cushion, Flotation

Product Code

KIC

Company Function(s)

Foreign Exporter, Specification Developer

Proprietary Name(s)

Prevasse

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