# Petermann GmbH

FEI: 3000266850
Status: Active
Establishment types: Manufacture Medical Device
Owner/operator: Petermann GmbH (#10023922)

Address: WAldweg 3, Dombuehl Bavaria, 91601, DE

Mandatory US Agent: Arjo, Inc.

## Products

Total registered: 1
Top product codes: IKX
Regulation §: 890.5050

Proprietary names: ArjoHuntleigh Maxionce

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223000266850%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3000266850