# BIONCISE NV

FEI: 3007513241
Status: Active
Establishment types: Export Device to the United States But Perform No Other Operation on Device; Manufacture Medical Device for Another Party (Contract Manufacturer); Manufacture Medical Device
Owner/operator: Bioncise NV (#10028101)

Address: Bodemstraat 16/3, Wellen Limburg, B-3830, BE

Mandatory US Agent: Cook Myosite

## Products

Total registered: 1
Top product codes: KNW
Regulation §: 876.1075

Proprietary names: Spirotome, Coramate

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223007513241%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3007513241