Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3010113295

FEI Number

3010113295

Entity Name

COSMADE BELGIUM BV

City/State/Country

Heist-op-den-Berg Antwerpen, BE

Establishment Address

Impulsstraat 3, Heist-op-den-Berg Antwerpen B-2220, BE

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

COSMADE BELGIUM BV (Owner Number: 10059063)

Owner / Operator Contact Address

Impulsstraat 3, Heist-op-den-Berg, BE-NOTA B-2220, BE

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

RID Super Max Solution

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
NXB	Dispenser, Solid Medication	Physical Medicine	Class 1	890.5050	2018-11-27
PUN	Lice Removal Kit Containing A Solution	General Hospital	Class 1	880.5960	2025-07-08

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

COSMADE BELGIUM BV

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

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K944481	Garan Scientific, Inc.	THE HEART PROTECTOR	1995-04-10

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3010113295. Last updated year: 2026. Please use registration number 3010113295 when referencing this establishment in official correspondence.