A.Medical
Медицинские товары и расходники, Латвия
A.Medical: компания в сфере «Медицинские товары и расходники», Kurzemes rajons, Латвия. Внесена в государственный реестр компаний.
- Type
- brand seeking distribution
- Location
- Kurzemes rajons, Latvia
- Founded
- 2012
- Categories
- Медицинские товары и расходники
Listed in a source registry
Latvia Register of Enterprises and State Revenue Service open data
Verified facts
- workforce-on-record (green), checked 2024-12-31 VID
- sanctions-clear (green), checked 2026-09-03 OpenSanctions
- debarment-clear (green), checked 2026-09-03 OpenSanctions
- tax-filing-active (green), checked 2024-12-31 VID
- public-contract-awarded (green), checked 2026-08-13 TED (Tenders Electronic Daily), EU public procurement award notices Здесь награда несёт ещё и чужую проверку: в ЕС и ЕЭЗ заказчик обязан отстранить участника, осуждённого за мошенничество, коррупцию или отмывание, и того, за кем окончательным решением признаны долги по налогам или социальным взносам. Directive 2014/24/EU, Article 57 (exclusion grounds)
- registry-active-global (green), checked 2026-08-31 Uzņēmumu reģistrs (Latvia)
- registered-since (green), checked 2012-10-23 Uzņēmumu reģistrs (Latvia)
- directors-on-file (green), checked 2026-08-31 Uzņēmumu reģistrs (Latvia)
- leadership-on-record (green), checked 2018-11-06 Uzņēmumu reģistrs (Latvia)
- ownership-on-record (green), checked 2026-08-31 Uzņēmumu reģistrs (Latvia)
- insolvency-clear (green), checked 2026-08-31 Uzņēmumu reģistrs (Latvia)
- registry-id-verified (green), checked 2026-07-08 Uzņēmumu reģistrs (Latvian Enterprise Register)
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)