PHARMAZEUTISCHE FABRIK MONTAVIT GES.M.B.H.

Listed in a source registry

US FDA device registration and listing (open.fda.gov)

Verified facts

• registered-manufacturer (green), checked 2026-08-21 ALIMS (Medicines and Medical Devices Agency of Serbia), register of medical-device manufacturers
• operating-permit (green), checked 2026-08-19 EudraGMDP manufacturing authorisation register (EMA)
• debarment-clear (green), checked 2026-08-15 OpenSanctions
• fda-registered (green), checked 2026-08-15 FDA
• sanctions-clear (green), checked 2026-08-15 OpenSanctions
• facility-registered (green), checked 2026-08-07 US FDA device establishment registration (openFDA)
• gmp-certified (green), checked 2024-07-18 EudraGMDP, EU register of GMP certificates (EMA)

Claimed certifications

• Good Manufacturing Practice
• FDA Registered FDA Establishment Registration

Import rules for these goods

• Medical devices sold in the EU must carry CE marking under the Medical Device Regulation (EU) 2017/745, with a conformity assessment matched to the device risk class. European Commission (MDR)
• For the US market, the maker must have an FDA device establishment registration and product listing; most instruments also need 510(k) premarket clearance. US FDA (devices)

Check independently

• Sanctions and watchlists (OpenSanctions)