FDA Registration Number: 3007238754

Last Validated: April 27, 2024

Status: Valid

Valid2024 U.S. FDA Medical Device Establishment Registration

LOPITAL NEDERLAND B.V.

Establishment Information

Laarakkerweg 9
Oisterwijk Noord-Brabant, NL 5061 JR
31-13-5239300

U.S. Agent

Registrar Corp
144 Research Drive
Hampton VA, USA 23666
+1-757-224-0177
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  
Lift, Patient, Non-Ac-Powered FSA Valid April 26, 2024

Device Listing

Device Name

Lift, Patient, Non-Ac-Powered

Product Code

FSA

Company Function(s)

Manufacturer

Proprietary Name(s)

Elexo XXL
6100 2060 Marina electric deLuxe
6100 2050 Marina electric basic
Flexo
Marina
6100 2000 Marina hydraulic basic
Elexo
Reflex
6100 2010 Marina hydraulic deluxe

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