# NUCLETRON B.V.

FEI: 3002807741
Status: Active
Establishment types: Export Device to the United States But Perform No Other Operation on Device; Develop Specifications But Do Not Manufacture At This Facility
Owner/operator: Nucletron B.V. (#8030474)

Address: 3900 AX VEENENDAAL, P.O. BOX 930, Waardgelder 1, VEENENDAAL Utrecht, 3905 TH, NL

Mandatory US Agent: Elekta

## Products

Total registered: 1
Top product codes: JAQ
Regulation §: 892.5700

Proprietary names: INTRACAVITARY MOULD APPLICATOR SET, INTRACAVITARY MOULD APPLICATOR SET Ft

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223002807741%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3002807741