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.
Sloveense industriële fabrikant en exporteur
LP MYCRON strojegradnja d.o.o. is door Sloexport genoteerd in de sector verspaning en metaalbewerking. Het directoryprofiel beschrijft onder meer de activiteiten van het bedrijf. De werking van het bedrijf kan worden gedefinieerd als de ontwikkeling van technologische processen en de productie van zeer veeleisende componenten, van prototype tot serie, in overeenstemming met de APQP-, FMEA-, PPAP-, SPC- en MSA-richtlijnen, die zijn ingebouwd in wereldberoemde merken van productiemachines, medische apparaten en voertuigen.
- 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
- Farmaceutische productie, Medische en gezondheidszorgbenodigdheden, Voertuigonderdelen en accessoires
- Markets
- Slovenië, Oostenrijk, Duitsland, Italië, Kroatië
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: Medische en gezondheidszorgbenodigdheden (the company's own text), Voertuigonderdelen en accessoires (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 Farmaceutische productie: 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
Before a first order, ask for the production site address and a document linking that site to this legal entity.