FDA Device Establishments · JSON-LD · Markdown

NUCLETRON B.V.

FEI 3002807741 · Export Device to the United States But Perform No Other Operation on Device Develop Specifications But Do Not Manufacture At This Facility · Status: Active

FEI Number3002807741
Owner / OperatorNucletron B.V. (#8030474)
Address3900 AX VEENENDAAL, P.O. BOX 930, Waardgelder 1, VEENENDAAL Utrecht, 3905 TH, NL
Mandatory US AgentElekta
Registration expiry2026
Initial importer flagN
Registered products1
Product codes (top 20)JAQ
Regulation § (21 CFR)892.5700
Proprietary namesINTRACAVITARY MOULD APPLICATOR SET; INTRACAVITARY MOULD APPLICATOR SET Ft

External sources

Source: openFDA. Public-domain (CC0).