FDA Device Establishments · JSON-LD · Markdown

PHILIPP KIRSCH GMBH

FEI 3043616309 · Manufacture Medical Device · Status: Active

FEI Number3043616309
Owner / OperatorPhilipp Kirsch GmbH (#10095114)
AddressIm Lossenfeld 14, Willstatt Baden-Wurttemberg, 77731, DE
Mandatory US AgentHettich Instruments
Registration expiry2026
Initial importer flagN
Registered products1
Product codes (top 20)KSE
Regulation § (21 CFR)864.9700
Proprietary namesFROSTER BL 730 US ULTIMATE; FROSTER BL 730 US PRO-ACTIVE; FROSTER BL 530 US PRO-ACTIVE; BL 520 US ULTIMATE; BL 720 US PRO-ACTIVE; BL 340 US ULTIMATE; FROSTER BL 330 US ULTIMATE; FROSTER BL 330 US PRO-ACTIVE; BL 300 US PRO-ACTIVE; BL 300 US ULTIMTAE

External sources

Source: openFDA. Public-domain (CC0).