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.
Fabricant industriel et exportateur slovène
LP MYCRON strojegradnja d.o.o. est référencée par Sloexport dans le secteur de l'usinage et du travail des métaux. Son profil d'annuaire décrit les opérations, notamment Le fonctionnement de l'entreprise peut être défini comme le développement de processus technologiques et la production de composants très exigeants, du prototype à la série, conformément aux directives APQP, FMEA, PPAP, SPC et MSA, qui sont intégrées dans des marques de renommée mondiale de machines de fabrication, de dispositifs médicaux et de véhicules.
- 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
- Production pharmaceutique, Fournitures médicales et de santé, Pièces et accessoires auto
- Markets
- Slovénie, Autriche, Allemagne, Italie, Croatie
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: Fournitures médicales et de santé (the company's own text), Pièces et accessoires auto (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 Production pharmaceutique: 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.