Biotronics Ltd
Life Science & Diagnostic Solutions Cyprus | Medical, Analytical, Laboratory Solutions Cyprus - Biot
Life Science & Diagnostic Solutions Cyprus | Medical, Analytical, Laboratory Solutions Cyprus
- Type
- Distributor
- Location
- Cyprus
- Website
- https://biotronics.com.cy
- Categories
- 医疗保健用品
- Markets
- 塞浦路斯
Verified facts
- named-by-manufacturer (green), checked 2026-08-24 Aerogen Ltd distributor list
- directors-on-file (green), checked 2026-08-19 Department of Registrar of Companies and Intellectual Property (Cyprus), open register bulk files via data.gov.cy
- public-contract-awarded (green), checked 2026-07-13 Treasury of the Republic of Cyprus, eProcurement register of awarded public contracts, via data.gov.cy 在这里，中标还附带了别人做过的审查：在欧盟和欧洲经济区，公共采购方必须排除因欺诈、腐败或洗钱被定罪的投标人，以及经终局裁决认定拖欠税款或社会保险费的投标人。 Directive 2014/24/EU, Article 57 (exclusion grounds)
- leadership-on-record (green), checked 2026-08-19 Department of Registrar of Companies and Intellectual Property (Cyprus), open register bulk files via data.gov.cy
- registered-address (green), checked 2026-08-19 Department of Registrar of Companies and Intellectual Property (Cyprus), open register bulk files via data.gov.cy
- registered-since (green), checked 2026-08-19 Department of Registrar of Companies and Intellectual Property (Cyprus), open register bulk files via data.gov.cy
- registry-active-global (green), checked 2026-08-19 Department of Registrar of Companies and Intellectual Property (Cyprus), open register bulk files via data.gov.cy
- registry-id-verified (green), checked 2026-08-19 Department of Registrar of Companies and Intellectual Property (Cyprus), open register bulk files via data.gov.cy
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)