FDA Registration Number: 3009540739

Last Validated: July 07, 2022

Status: Valid

Valid2022 U.S. FDA Medical Device Establishment Registration

CANDOR APS

Establishment Information

Sandagervej 18b
Gislev Syddanmark, DK DK-5854

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  
Support, Patient Position CCX Valid July 06, 2022

Device Listing

Device Name

Support, Patient Position

Product Code

CCX

Company Function(s)

Foreign Exporter, Manufacturer

Proprietary Name(s)

Combi Board

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