# TissueGUARD

FEI: 3031572059
Status: Active
Establishment types: Complaint File Establishment per 21 CFR 820.198; Manufacture Medical Device
Owner/operator: TissueGUARD GmbH (#10090875)

Address: Hohe Str 6, Dresden Saxony, 01069, DE

Mandatory US Agent: EMG Consulting Services

## Products

Total registered: 1
Top product codes: HMX
Regulation §: 886.4350

Proprietary names: TissueGUARD DMEK Injector SET

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223031572059%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3031572059