# PURTEX S.R.O.

FEI: 3038188186
Status: Active
Establishment types: Manufacture Medical Device
Owner/operator: PURTEX s.r.o. (#10092884)

Address: Ustecka 103, Zdiby Praha-Vychod, 25066, CZ

Mandatory US Agent: MAK and Associates, LLC

## Products

Total registered: 1
Top product codes: FNM
Regulation §: 880.5550

Proprietary names: HybriMatt 200

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223038188186%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3038188186