# DRG INSTRUMENTS GMBH

FEI: 3002800697
Status: Active
Establishment types: Complaint File Establishment per 21 CFR 820.198; Manufacture Medical Device
Owner/operator: BIOCHECK, INC. (#9033543)

Address: FRAUENBERGSTRASSE 18, MARBURG Hesse, D-35039, DE

Mandatory US Agent: DRG International, Inc.

## Products

Total registered: 1
Top product codes: JKD
Regulation §: 862.1135

Proprietary names: C-Peptide ELISA, Insulin (human) Ultrasensitive ELISA

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223002800697%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3002800697