LP MYCRON strojegradnja d.o.o.
Company-provided description, not an official-source fact. Certifications, capacities, years and market positions stated in it are the company's own claims until a record below confirms them.
Fabricante y exportador industrial esloveno
LP MYCRON strojegradnja d.o.o. cotiza en Sloexport en el sector de mecanizado y metalmecánica. Su perfil de directorio describe operaciones que incluyen El funcionamiento de la empresa se puede definir como el desarrollo de procesos tecnológicos y la producción de componentes altamente exigentes desde el prototipo hasta la serie de acuerdo con las directrices APQP, FMEA, PPAP, SPC y MSA, que están integradas en marcas de fabricación de máquinas, dispositivos médicos y vehículos de renombre mundial.
- Type
- Not established by any record (our catalog import lists it as manufacturer; that is not evidence of the role)
- Role
- Role not established by any record
- Location
- Ptuj, Slovenia
- Founded
- 1994 (as stated by the company, not confirmed by a state register)
- Website
- https://lp-mycron.eu
- Categories
- Fabricación farmacéutica, Suministros médicos y sanitarios, Piezas y accesorios para vehículos
- Markets
- Eslovenia, Austria, Alemania, Italia, Croacia
Listed in a source registry
What is established and what is not
No researcher review has been written for this company yet. 4 official records from 4 official sources are on file. Everything is listed below with its evidence type: each entry confirms only what it literally says; none of them is a review. Nothing here confirms manufacturing, ownership or trading status beyond what each record literally says.
Facts on file, each with its evidence type
- EU customs identifier (EORI) active (record type: export-registered-eori) [official record; status green] An EORI number identifies the company to EU customs for imports, exports and transit. A valid number does not show that any shipment took place and is not a licence to export a particular product. checked 2026-07-30. EU EORI validation (European Commission)
- registry-activity (record type: registry-activity) [official record; status green] Shows what the state itself says the company does, which you can compare with what it promises you. checked 2026-08-16. Seznam davčnih zavezancev (FURS, Finančna uprava RS)
- Registry ID checks out with the state register (record type: registry-id-verified) [official record; status green] Helps confirm the company on this page is the same legal entity as in the register. checked 2026-08-16. Poslovni register Slovenije (AJPES)
- EU VAT number valid for cross-border trade (record type: vat-valid) [official record; status green] The number is registered and active: we asked the EU VIES service and it answered yes. An invalid VAT number is the first sign an invoice comes from the wrong company. 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)
- Vehicle parts affecting safety sold in Europe generally require UNECE type approval (E-mark). UNECE
Goods family established: Suministros médicos y sanitarios (the company's own text), Piezas y accesorios para vehículos (the company's own text). The exact product, operation and trade route needed to determine a product-specific requirement are not established here. Product-specific import rules not established for the catalog category Fabricación farmacéutica: no record or company text names goods of this kind. A catalog category alone is our classification, not proof of what the company makes or sells.
Check independently
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