# Dreve Otoplastik GmbH

FEI: 3003610251
Status: Active
Establishment types: Manufacture Medical Device for Another Party (Contract Manufacturer); Manufacture Medical Device
Owner/operator: DREVE OTOPLASTIK GMBH (#9028387)

Address: MAX-PLANCK-STR. 31, UNNA North Rhine-Westphalia, 59423, DE

Mandatory US Agent: DREVE AMERICA CORP.

## Products

Total registered: 1
Top product codes: ESD
Regulation §: 874.3300

Proprietary names: Otopren, Tube end piece, Biopor AB, Fotoplast S hart, Biopor AB Xtrack, Thermosoft Lack, Fotoplast S IO lv, Biopor AB fluoreszent, BioTec, FotoTec Repair

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223003610251%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3003610251