# ALLWIN MEDICAL DEVICES, INC.

FEI: 3005987240
Status: Active
Establishment types: Repack or Relabel Medical Device
Owner/operator: ALLWIN MEDICAL DEVICES, INC. (#9094082)

Address: 3305 E. MIRALOMA AVENUE, SUITE 176, ANAHEIM, CA, US



## Products

Total registered: 1
Top product codes: EZB
Regulation §: 876.5130

Proprietary names: KING COBRA Nitinol Guidewire, Standard Straight Tip Guidewire, HYGUIDE Hydrophilic Guidewire, COBRA Nitinol Guidewire, LUNDERQUIST Guidewire, Standard J Tip Guidewire, SCHULLER Guidewire, SUPREMO Nitinol Hydrophilic Guidewire

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223005987240%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3005987240