Lohmann & Rauscher GmbH

Listed in a source registry

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

Verified facts

• public-contract-awarded (green), checked 2026-08-02 TED, EU public procurement bulletin Here the award carries someone else's check: in the EU and the EEA a public buyer must exclude bidders convicted of fraud, corruption or money laundering, and those found by a final decision to owe taxes or social contributions. Directive 2014/24/EU, Article 57 (exclusion grounds)
• lei-lapsed (amber), checked 2026-08-15 GLEIF
• sanctions-clear (green), checked 2026-08-15 OpenSanctions
• fda-registered (green), checked 2026-08-15 FDA
• debarment-clear (green), checked 2026-08-15 OpenSanctions
• export-registered (green), checked 2026-08-07 US FDA device establishment registration (openFDA)
• facility-registered (green), checked 2026-08-07 US FDA device establishment registration (openFDA)

Claimed certifications

• 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)