LP MYCRON strojegradnja d.o.o.
Fabricante e exportador industrial esloveno
LP MYCRON strojegradnja d.o.o. é listada pela Sloexport no setor de usinagem e metalurgia. Seu perfil de diretório descreve operações, incluindo A operação da empresa pode ser definida como o desenvolvimento de processos tecnológicos e produção de componentes altamente exigentes, do protótipo à série, de acordo com as diretrizes APQP, FMEA, PPAP, SPC e MSA, que são incorporadas em marcas de renome mundial de máquinas de fabricação, dispositivos médicos e veículos.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Ptuj, Slovenia
- Founded
- 1994
- Website
- https://lp-mycron.eu
- Categories
- Fabricação farmacêutica, Suprimentos médicos e de saúde, Peças e acessórios para veículos
- Markets
- Eslovênia, Áustria, Alemanha, Itália, Croácia
Listed in a source registry
What is established and what is not
No facet of this company has been investigated yet. The facts below are collected records, not an assessment: nothing here confirms manufacturing, ownership or trading status beyond what each record literally says.
Verified facts
- export-registered (green), checked 2026-07-30 EU EORI validation (European Commission)
- registry-activity (green), checked 2026-08-16 Seznam davčnih zavezancev (FURS, Finančna uprava RS)
- registry-id-verified (green), checked 2026-08-16 Poslovni register Slovenije (AJPES)
- vat-valid (green), checked 2026-08-01 VIES (European Commission)
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)
- 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)
- Vehicle parts affecting safety sold in Europe generally require UNECE type approval (E-mark). UNECE