LP MYCRON strojegradnja d.o.o.
Slovenian industrial manufacturer and exporter
LP MYCRON strojegradnja d.o.o. is listed by Sloexport in the machining and metalworking sector. Its directory profile describes operations including The operation of the company can be defined as the development of technological processes and production of highly demanding components from prototype to series in accordance with APQP, FMEA, PPAP, SPC and MSA guidelines, which are built into world-renowned brands of manufacturing machines, medical devices and vehicles.
- 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
- Pharmaceutical Manufacturing, Medical & Healthcare Supplies, Vehicle Parts & Accessories
- Markets
- Slovenia, Austria, Germany, Italy, Croatia
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