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
- 医療およびヘルスケア用品
- Markets
- キプロス
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 ここでの落札は、他者による審査も伴います。EUおよびEEAでは、公共調達者は詐欺、汚職、資金洗浄で有罪となった入札者、および確定した決定で税や社会保険料の未納が認定された入札者を排除しなければなりません。 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)