Establishment registration

GEUDER AG

FDA establishment registration 9616245 · HEIDELBERG Baden-Wurttemberg, DE

Key facts

Registration number 9616245
Establishment name GEUDER AG
Owner/operator GEUDER AG
Owner/operator number 9024476
FEI number 3003408840
Address HERTZSTRASSE 4
City HEIDELBERG Baden-Wurttemberg
Country DE
Registration valid through 2026
Product codes listed HLE, HMR, HMX, HNA, HNB, HNC, HND, HNE, HNF, HNH, HNI, HNJ, HNK, HNL, HNN, HNQ, HNR, HNX, HNZ, HOB, HOC, HOD, HOE, HPN, HRH, KYG, NCE, NGY
Device classes 1

At a glance

  • 10–99 Device listings
  • 1–9 UDI devices (GUDID)
  • Current Registration current
  • None FDA inspections at this FEI

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA device establishment registrations

Device establishments that manufacture, repackage, relabel or import devices for the U.S. market must register annually with the FDA and list the devices they produce.

Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database

Browse all FDA device establishment registrations