FDA Device Establishments · JSON-LD · Markdown

SCHEBO BIOTECH AG

FEI 3003780132 · Manufacture Medical Device Complaint File Establishment per 21 CFR 820.198 · Status: Active

FEI Number3003780132
Owner / OperatorSCHEBO BIOTECH AG (#9032007)
AddressNETANYASTRASSE 3-5, GIESSEN Hesse, 35394, DE
Mandatory US AgentSCHEBO BIOTECH USA, INC.
Registration expiry2026
Initial importer flagN
Registered products1
Product codes (top 20)JCC
Regulation § (21 CFR)864.4010
Proprietary namesScheBo Extraction Buffer 5X; Extraction Buffer 5X

External sources

Source: openFDA. Public-domain (CC0).