k+ s minerals and agriculture gmbh
K+S Aktiengesellschaft
We promote life for generations. The listed German mining company K+S introduces itself
- Type
- Manufacturer
- Location
- Kassel, Germany
- Founded
- 2002
- Website
- https://www.kpluss.com
- Categories
- Pharmaceutical Manufacturing, Chemicals & Plastics, Medical & Healthcare Supplies
Listed in a source registry
Verified facts
- domain-registered (green), checked 2026-08-09 Domain registry record
- debarment-clear (green), checked 2026-08-09 OpenSanctions
- vat-valid (green), checked 2026-08-13 VIES (European Commission)
- sanctions-clear (green), checked 2026-08-09 OpenSanctions
- lei-active (green), checked 2026-08-23 GLEIF global LEI register (golden copy)
- gmp-certified (green), checked 2026-01-27 EudraGMDP, EU register of GMP certificates (EMA)
- facility-registered (green), checked 2026-08-16 European Industrial Emissions Portal (E-PRTR / IED), European Environment Agency
- operating-permit (green), checked 1998-07-24 EEA Industrial Emissions Portal (IED), EU-wide permit register
- aeo-certified (green), checked 2026-08-16 EU AEO register (European Commission)
- registry-active-global (green), checked 2026-08-17 Marktstammdatenregister (Bundesnetzagentur)
- registered-since (green), checked 2002-01-01 Marktstammdatenregister (Bundesnetzagentur)
Profiles
Claimed certifications
- Good Manufacturing Practice
- 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)
- Chemical substances imported into the EU above 1 tonne/year must be REACH-registered. ECHA (REACH)
- Medicines imported into the EU must come from a site holding an EU GMP certificate, and the importer needs a manufacturing/import authorisation. European Medicines Agency (GMP)