Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3007238754

FEI Number

3007238754

Entity Name

LOPITAL NEDERLAND B.V.

City/State/Country

Oisterwijk Noord-Brabant, NL

Establishment Address

Laarakkerweg 9, Oisterwijk Noord-Brabant 5061 JR, NL

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Lopital Nederland B.V. (Owner Number: 10039562)

Owner / Operator Contact Address

Laarakkerweg 9, Oisterwijk, NL-NB 5061 JR, NL

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Elexo XXL Marina Flexo Reflex 6100 2060 Marina electric deLuxe 6100 2050 Marina electric basic 6100 2010 Marina hydraulic deluxe Elexo 6100 2000 Marina hydraulic basic Timo Shower-toilet chair 6035 Timo Shower-toilet chair 6030 Vienna basic fixed height Nemo Tango XXL Lotus Tango Tango XL Lotus XL Timo Shower-Toilet chair 6021 Timo Shower chair 6020 Stylex Sirocco basic fix height Amfora Lotus compact

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
FSA	Lift, Patient, Non-Ac-Powered	General Hospital	Class 1	880.5510	2012-01-24

Official Correspondent

No official correspondent registered.

US Agent Details

David Lennarz Business: Registrar Corp Email: david.lennarz@registrarcorp.com Phone: (757) 2240177

Related Public Records

Same Entity

Lopital Nederland B.V.

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0013-2018	Handicare Usa Inc	1	PRISM MEDICAL A-625, MAX. LOAD 625 lbs. 283 Kgs., Patient lift, non-A/C powered
Z-0014-2018	Handicare AB Maskinvagen	1	Carina Mobile Lifts, Models: a) Carina350EM, REF 6060011 b) Carina350EML, REF 60600012 c) Carina350EE, REF 60600009

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3007238754. Last updated year: 2026. Please use registration number 3007238754 when referencing this establishment in official correspondence.