# Arvato SE

FEI: 3013247477
Status: Active
Establishment types: Repack or Relabel Medical Device
Owner/operator: Arvato SE (#10053073)

Address: Werner-Schroeder Str 1, Hamburg, 21035, DE

Mandatory US Agent: Gyrus ACMI, Inc.

## Products

Total registered: 1
Top product codes: PMU
Regulation §: 884.4050

Proprietary names: Containment system, laparoscopic power morcellation, with instrument port

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223013247477%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3013247477