# HEMEDEX INCORPORATED

FEI: 3003730855
Status: Active
Establishment types: Manufacture Medical Device
Owner/operator: HEMEDEX INCORPORATED (#9048090)

Address: 564 Main Street, Suite 300, North Waltham, MA, US



## Products

Total registered: 2
Top product codes: HBG, GWM
Regulation §: 882.4300, 882.1620

Proprietary names: QFLOW 500TM TITANIUM BOLT Dual Lumen, QFLOW 500TM TITANIUM BOLT Single Lumen Bolt Kit with Dura Piercer, QFLOW 500TM 5.3 mm Cranial Drill Bit, QFLOW 500TM TITANIUM BOLT Dual Lumen Bolt Kit, QFLOW 500TM TITANIUM BOLT Quad Lumen Bolt Kit, QFLOW 500TM TITANIUM BOLT Single Lumen, QFLOW 500TM 2.7 mm Cranial Drill Bit, QFLOW 500TM Accessories, Touhy Borst / Compression Fitting 0-9 FR, QFLOW 500TM TITANIUM BOLT Dual Lumen Bolt Kit with Introducer, QFLOW 500TM Accessories, Bolt Accessories Kit

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223003730855%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3003730855