seca
医療機器、ヘルスケア用品、臨床製品。
seca はハンブルクの事業所で医療機器、ヘルスケア用品、臨床製品を製造しています。同社は、病院のバイヤー、臨床販売代理店、ヘルスケア システム、または上場主要市場全体の輸出顧客に製品を供給しています。
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Hamburg, Germany
- Founded
- 1840
- Website
- seca.com
- Categories
- 医療およびヘルスケア用品, 産業用品
- Markets
- ドイツ, アメリカ合衆国, 中国, 日本
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
- sanctions-clear (green), checked 2026-08-03 OpenSanctions
- fda-registered (green), checked 2026-08-03 FDA
- web-presence-since (green), checked 2026-08-03 Internet Archive (Wayback)
- lei-lapsed (amber), checked 2026-08-03 GLEIF
- debarment-clear (green), checked 2026-08-03 OpenSanctions
- domain-registered (green), checked 2026-08-03 Domain registry record
- vat-valid (green), checked 2026-08-03 VIES
- corporate-mail-on-domain (green), checked 2026-08-03 Mail server of the company domain
- registered-manufacturer (green), checked 2026-09-17 Ministero della Salute, banca dati e Repertorio dei dispositivi medici
Profiles
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)