# Gebr. Schwarz GmbH

FEI: 3012055599
Status: Active
Establishment types: Manufacture Medical Device for Another Party (Contract Manufacturer); Repack or Relabel Medical Device
Owner/operator: Gebr. Schwarz GmbH (#10051999)

Address: Zepfenhaner Strabe 35, Rottweil Baden-Wurttemberg, 78628, DE

Mandatory US Agent: Aesculap, Inc.

## Products

Total registered: 1
Top product codes: KCT
Regulation §: 880.6850

Proprietary names: Sterilization locks

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223012055599%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3012055599