# ORBUSNEICH MEDICAL CO. LTD (HONG KONG)

FEI: 3015002281
Status: Active
Establishment types: Export Device to the United States But Perform No Other Operation on Device
Owner/operator: OrbusNeich Medical Co. Ltd (Hong Kong) (#10059958)

Address: Units 303 &305, 3/F, Building 20E, Hong Kong Science Park, Shatin, N.t., Hong Kong, No. 27-31 Au Pui Wan Streeet, Fo Tan, N.T., NA, HK

Mandatory US Agent: OrbusNeich Medical, Inc.

## Products

Total registered: 2
Top product codes: LIT, LOX
Regulation §: 870.1250, 870.5100

Proprietary names: Sapphire II Pro Coronary Dilatation Catheter

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223015002281%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3015002281