Abionic SA
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.
에이비오닉
소아용으로 승인된 PSP PSP는 이제 신생아부터 성인까지 조기 패혈증 감지를 지원하여 간병인이 지체 없이 최적의 치료 프로토콜을 실행할 수 있도록 지원합니다! 병원 업무 흐름 전반에 걸친 패혈증 조기 감지 패혈증은 신속한 규칙 적용이 필요한 시간에 민감한 응급 상황입니다. 응급 및 중환자 치료 환경에는 표준 치료보다 조기에 패혈증을 감지할 수 있는 솔루션이 필요합니다. abioSCOPE®에서만 측정된 PSP(췌장 결석 단백질) 바이오마커는 간병인이 몇 분 안에 패혈증을 감지하고 활성화할 수 있도록 해줍니다. 자세히... abioSCOPE® 환자에 가까운 신속한 진단 플랫폼인 abioSCOPE®는 임상 작업 흐름에 원활하게 통합되고 몇 분 안에 혈액 한 방울로 실험실 수준의 결과를 제공하여 귀중한 임상 통찰력을 제공합니다. 더..
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer (official record)
- Location
- Epalinges, Switzerland
- Website
- https://abionic.com
- Categories
- 의료 및 건강 관리 용품
Listed in a source registry
What is established and what is not
No researcher review has been written for this company yet. 5 official records from 5 official sources are on file. 4 other entries are not official records: our own technical checks and searches, open directory listings, our inferences or the company's own statements. Everything is listed below with its evidence type: each entry confirms only what it literally says; none of them is a review. The manufacturing role above rests on the official records listed below, and only as far as each literally goes: a facility registration or licence is not an observation of current production. Nothing here confirms ownership or trading status beyond what each record literally says.
Facts on file, each with its evidence type
- Business email on the company's own domain (record type: corporate-mail-on-domain) [our own observation, not an official record; status green] Shows the domain runs its own email rather than a free mailbox. It describes the domain, not who owns it. checked 2026-08-22. Mail server of the company domain
- Website domain registered (record type: domain-registered) [our own observation, not an official record; status green] Shows how long this web address has been registered. That is the age of the domain, not of the company: a domain can change owners. checked 2026-08-22. Domain registry record
- No match found in the debarment registers we checked (record type: debarment-clear) [our own observation, not an official record; name search, no matching candidate] We searched the public debarment datasets and found no matching candidate. Absence from these lists is a search result, not a certificate. checked 2026-08-22. OpenSanctions
- Registered with the U.S. FDA (active, renewed for the current year) (record type: fda-registered) [official record; status green] Registered with the US food and drug regulator, renewed for the current year. checked 2026-08-22. FDA
- Legally registered and still active (record type: registry-active-global) [official record; status green] Shows the register lists the registration as active on the date we read it. It does not show how busy the business is. checked 2026-08-22. Zefix (Swiss commercial registry)
- No match found on the sanctions lists we checked (record type: sanctions-clear) [our own observation, not an official record; name search, no matching candidate] We searched the public sanctions datasets and found no matching candidate. A name search is not full compliance screening. checked 2026-08-22. OpenSanctions
- Legal entity ID lapsed (record type: lei-lapsed) [official record; status amber] The global finance identifier was not renewed. This does not mean the company closed. checked 2026-08-22. GLEIF
- Registered as a manufacturer (record type: registered-manufacturer) [official record; status green] Its own declared activity in the register covers making these goods. checked 2026-10-17. Swissmedic, swissdamed register of Swiss and Liechtenstein economic operators for medical devices
- product-authorised-for-sale-holder (record type: product-authorised-for-sale-holder) [official record; status green] Applicant to the US FDA for 1 medical devices: IVD CAPSULE PSP; abioSCOPE (K240041, 2024-09-25). The applicant answers for the notification; the record does not say who makes the device. A national regulator lists this company as the holder of the registration of products it has authorised for sale in that country. The holder answers for the product on that market; the record does not say the holder makes it. effective since 2026-10-05. FDA premarket notifications 510(k) and De Novo (openFDA, U.S. Food and Drug Administration)
Relationships
1 relationship(s) on file. Each line names the other party, the relationship as its source records it, and the source. A record of a relationship is not a finding about control beyond what it literally says.
Candidates, not confirmed
- abionic.com: Website of this business. Source 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)