FDA Device Establishments · JSON-LD · Markdown

Teleflex Medical Inc.

FEI 3012481535 · Develop Specifications But Do Not Manufacture At This Facility · Status: Active

FEI Number3012481535
Owner / OperatorTeleflex (#9062981)
Address4300 Glendale Milford Road, Cincinnati, OH, US
Registration expiry2026
Initial importer flagN
Registered products1
Product codes (top 20)KNT
Regulation § (21 CFR)876.5980
Proprietary namesStandard Precision Bougie Device; Standard Tapered Bougie, 38 Fr (STB38)

External sources

Source: openFDA. Public-domain (CC0).