FDA Device Establishments · JSON-LD · Markdown

BIVIAX GMBH & CO KG

FEI 3009308084 · Manufacture Medical Device · Status: Active

FEI Number3009308084
Owner / Operatorbiviax GmbH & Co KG (#10037830)
AddressHagener Strasse 428, Dortmund North Rhine-Westphalia, 44229, DE
Mandatory US AgentPauly P.A.
Registration expiry2026
Initial importer flagN
Registered products1
Product codes (top 20)HXT
Regulation § (21 CFR)878.4800
Proprietary namesK-Tape; K-Tape My Skin; K-Tape Pure; CROSSTAPE

External sources

Source: openFDA. Public-domain (CC0).