Medicop specialna oprema d.o.o.
Produsen dan eksportir industri Slovenia
Medicop specialna oprema d.o.o. terdaftar oleh Sloexport di sektor manufaktur lainnya. Profil direktorinya menjelaskan operasi termasuk Perusahaan Medicop dari Murska Sobota yang bergerak dalam produksi peralatan medis dan perlengkapan kendaraan untuk tujuan khusus. Pengalaman bertahun-tahun dan kerjasama dengan pengguna di bidang peralatan medis di bidang gas medis di rumah sakit dan ambulans memungkinkan kami untuk menciptakan manusia profesional yang terbaik.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Murska Sobota, Slovenia
- Website
- https://medicop.eu
- Categories
- Manufaktur Farmasi, Perlengkapan Medis & Kesehatan, Suku Cadang & Aksesori Kendaraan
- Markets
- Slovenia, Austria, Jerman, Italia, Kroasia
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
- public-contract-awarded (green), checked 2026-08-03 TED, EU public procurement bulletin Di sini kemenangan tender juga membawa pemeriksaan pihak lain: di UE dan EEA, pembeli publik wajib menggugurkan peserta yang dipidana karena penipuan, korupsi, atau pencucian uang, serta yang tunggakan pajak atau iurannya ditetapkan lewat putusan final. Directive 2014/24/EU, Article 57 (exclusion grounds)
- lei-lapsed (amber), checked 2026-09-07 GLEIF global LEI register (golden copy)
- registry-id-verified (green), checked 2026-09-10 GLEIF Global LEI record
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