FDA Device Establishments · JSON-LD · Markdown

Life Technologies Corporation

FEI 3003335080 · Manufacture Medical Device · Status: Active

FEI Number3003335080
Owner / OperatorLife Technologies Corporation (#9915045)
Address7335 Executive Way, FREDERICK, MD, US
Registration expiry2026
Initial importer flagY
Registered products1
Product codes (top 20)PFT
Regulation § (21 CFR)862.3800
Proprietary namesDS-33 Matrix Standard (Dye Set G5) Dx; Cathode Buffer Container Dx; POP-7™ Polymer Dx (960 Samples); DS-33 GeneScan™ Install Kit Dx with GeneScan™ 600 LIZ™ v2; DynaMag™ 16-2mL Tube Dx; Ion OneTouch™ Dx Template Solutions; Ion PGM™ Dx Library Reagents; Ion PGM™ Dx Library Equalizer; DynaMag™ 96-Well Plate Dx, 5-200 uL; Polymer Pouch Caps, Dx

External sources

Source: openFDA. Public-domain (CC0).