Venture Corporation
Технологические решения для проектирования продукции, производства и цепочки поставок.
Венчурная корпорация предоставляет услуги по индустриализации продукции, производству электроники и цепочке поставок для технологических клиентов. Группа со штаб-квартирой в Сингапуре обслуживает рынки медико-биологических, промышленных, испытательных и измерительных, сетевых и потребительских технологий.
- Type
- brand seeking distribution
- Location
- Singapore
- Founded
- 1989
- Website
- venture.com.sg
- Categories
- Бытовая электроника, Медицинские товары и расходники, Промышленные станки и машины
- Markets
- Сингапур, Соединенные Штаты, Германия, Китай
Verified facts
- domain-registered (green), checked 2026-08-10 Domain registry record
- corporate-mail-on-domain (green), checked 2026-08-10 Mail server of the company domain
- fda-registered (green), checked 2026-08-10 FDA
- fda-contract-manufacturer (green), checked 2026-08-10 FDA
- certificate-page-on-site (amber), checked 2026-08-11 Company's own certification page
- registry-activity (green), checked 1984-08-04 ACRA Information on Corporate Entities (data.gov.sg)
- lei-active (green), checked 2026-08-30 GLEIF global LEI register (golden copy)
- debarment-clear (green), checked 2026-08-10 OpenSanctions
- sanctions-clear (green), checked 2026-08-10 OpenSanctions
- registered-since (green), checked 1984-08-04 ACRA Information on Corporate Entities (data.gov.sg)
Claimed certifications
- ISO 9001, Quality Management IAF CertSearch
- ISO 13485, Medical Devices Quality IAF CertSearch
- ISO 14001, Environmental Management IAF CertSearch
- FDA Registered FDA Establishment Registration
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)
- Electronics for the EU need CE marking incl. RoHS substance limits, and producers must register for WEEE take-back in each member state of sale. European Commission (CE)
- Electronics for the US market need FCC equipment authorization under 47 CFR Part 15, which covers unintentional radiators such as switch-mode power supplies, not only radio devices. US FCC (Part 15)