Haemonetics
Medische apparaten, gezondheidszorgbenodigdheden en klinische producten.
Haemonetics produceert medische apparatuur, gezondheidszorgbenodigdheden en klinische producten vanuit haar activiteiten in Boston. Het bedrijf levert aan ziekenhuiskopers, klinische distributeurs, gezondheidszorgsystemen en exportklanten op zijn beursgenoteerde primaire markten.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Boston, United States
- Founded
- 1971
- Website
- haemonetics.com
- Categories
- Medische en gezondheidszorgbenodigdheden, Industriële benodigdheden
- Markets
- Verenigde Staten, Duitsland, Japan, Brazilië
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
- corporate-mail-on-domain (green), checked 2026-08-08 Mail server of the company domain
- domain-registered (green), checked 2026-08-08 Domain registry record
- web-presence-since (green), checked 2026-08-08 Internet Archive (Wayback)
- fda-registered (green), checked 2026-08-08 FDA
- sanctions-clear (green), checked 2026-08-08 OpenSanctions
- debarment-clear (green), checked 2026-08-08 OpenSanctions
- lei-active (green), checked 2026-09-07 GLEIF global LEI register (golden copy)
- certificate-page-on-site (amber), checked 2026-09-18 Company's own certification page
- registry-id-verified (green), checked 2026-09-10 GLEIF Global LEI record
Claimed certifications, not confirmed by us
- ISO 13485, Medical Devices Quality IAF CertSearch
- CE Marking EU NANDO (notified bodies)
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)