FDA Device Establishments · JSON-LD · Markdown

ALLWIN MEDICAL DEVICES, INC.

FEI 3005987240 · Repack or Relabel Medical Device · Status: Active

FEI Number3005987240
Owner / OperatorALLWIN MEDICAL DEVICES, INC. (#9094082)
Address3305 E. MIRALOMA AVENUE, SUITE 176, ANAHEIM, CA, US
Registration expiry2026
Initial importer flagN
Registered products1
Product codes (top 20)EZB
Regulation § (21 CFR)876.5130
Proprietary namesKING 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

External sources

Source: openFDA. Public-domain (CC0).