FDA Device Establishments · JSON-LD · Markdown
FEI 3012055599 · Manufacture Medical Device for Another Party (Contract Manufacturer) Repack or Relabel Medical Device · Status: Active
| FEI Number | 3012055599 |
|---|---|
| Owner / Operator | Gebr. Schwarz GmbH (#10051999) |
| Address | Zepfenhaner Strabe 35, Rottweil Baden-Wurttemberg, 78628, DE |
| Mandatory US Agent | Aesculap, Inc. |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | KCT |
| Regulation § (21 CFR) | 880.6850 |
| Proprietary names | Sterilization locks |
Source: openFDA. Public-domain (CC0).