KNAUER Wissenschaftliche Geräte GmbH
HPLC systems and chromatography instruments for labs.
KNAUER is a Berlin-based manufacturer of HPLC systems, pumps, detectors, and preparative chromatography equipment for pharmaceutical, biotech, and analytical chemistry laboratories. The family-owned company has supplied lab instruments to researchers and QC labs in over 50 countries since 1962.
- Type
- Manufacturer
- Location
- Berlin, Germany
- Founded
- 1962
- Website
- knauer.net
- Categories
- Industrial Machinery, Medical & Healthcare Supplies
- Markets
- Germany, United States, China, India, France
Verified facts
- lei-active (green), checked 2026-08-23 GLEIF global LEI register (golden copy)
- sanctions-clear (green), checked 2026-08-16 OpenSanctions
- debarment-clear (green), checked 2026-08-16 OpenSanctions
- public-contract-awarded (green), checked 2024-06-11 TED (Tenders Electronic Daily), EU public procurement award notices 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)
- aeo-certified (green), checked 2026-08-16 EU AEO register (European Commission)
- domain-registered (green), checked 2026-08-02 Domain registry record
- registry-active-global (green), checked 2026-08-17 Marktstammdatenregister (Bundesnetzagentur)
- vat-valid (green), checked 2026-08-01 VIES (European Commission)
Claimed certifications
- ISO 9001, Quality Management IAF CertSearch
- ISO 13485, Medical Devices Quality IAF CertSearch
- AEO, Authorised Economic Operator EU AEO database
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)
- Machinery sold in the EU needs CE marking with a declaration of conformity under the EU machinery rules. European Commission