# HUBERT DE BACKER N.V.

FEI: 3003192903
Status: Active
Establishment types: Manufacture Medical Device
Owner/operator: Hubert De Backer n.v. (#10032923)

Address: Laagstraat 59, Temse Oost-Vlaanderen, 9140, BE

Mandatory US Agent: P/L Biomedical

## Products

Total registered: 1
Top product codes: KYX
Regulation §: 880.6430

Proprietary names: T2248, T2188+T2187, T2249, T2044+T2043/A, T2120+T2064/A, T1959, T1630/2B, T1703/1+T2194/1, T2148/1, T1631/1

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223003192903%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3003192903