# MIE GMBH

FEI: 3005128583
Status: Active
Establishment types: Remanufacture Medical Device; Manufacture Medical Device
Owner/operator: MIE GMBH (#9028781)

Address: HAUPTSTR. 112, SETH Schleswig-Holstein, 23845, DE

Mandatory US Agent: MiE America Inc.

## Products

Total registered: 1
Top product codes: KPS
Regulation §: 892.1200

Proprietary names: ECAM SCINTRON

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223005128583%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3005128583