The Origin Foods Sdn Bhd
Fabricant malaisien d'agropyre, fonctionnel & nutraceutique, détoxification & gestion du poids, bio
The Origin Foods Sdn Bhd fabrique de l'herbe de blé, des produits fonctionnels et nutraceutiques, de désintoxication et de gestion du poids, des boissons bio, de la nutrition et de l'alimentation, de la santé des femmes, à Puchong, en Malaisie. La société a été créée en 1999 et fournit des clients professionnels en Malaisie et sur les marchés régionaux.
- Type
- brand seeking distribution
- Location
- Puchong, Malaysia
- Founded
- 1999
- Website
- originfoods.com.my
- Categories
- Épicerie sèche, Fournitures médicales et de santé
- Markets
- Malaisie, Singapour
Verified facts
- web-presence-since (green), checked 2026-08-04 Internet Archive (Wayback)
- corporate-mail-on-domain (green), checked 2026-08-09 Mail server of the company domain
- debarment-clear (green), checked 2026-08-09 OpenSanctions
- sanctions-clear (green), checked 2026-08-09 OpenSanctions
- standards-mark-certified (green), checked 2026-08-16 EAEU unified register of certificates and declarations
- facility-registered (green), checked 2026-08-19 BPOM (Indonesian Food and Drug Authority), public register of manufacturing facilities behind product registrations (Sarana)
Claimed certifications
- EAC mark (EAEU conformity) EAEU unified register of certificates and declarations
Import rules for these goods
- EU imports of food of animal origin and many other food categories must be pre-notified in TRACES and enter through border control posts. European Commission (TRACES)
- US imports require the foreign facility to be FDA-registered and the importer to run a Foreign Supplier Verification Program (FSVP). US FDA
- 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)