# DORNIER MEDTECH GMBH

FEI: 3002806833
Status: Active
Establishment types: Complaint File Establishment per 21 CFR 820.198
Owner/operator: DORNIER MEDTECH  GMBH (#8010622)

Address: ARGELSRIEDER FELD 7, WESSLING Bavaria, D-82234, DE

Mandatory US Agent: DORNIER MEDTECH AMERICA, INC.

## Products

Total registered: 1
Top product codes: LNS
Regulation §: 876.5990

Proprietary names: Gemini 220 XP

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223002806833%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3002806833