Kerala Ayurveda Ltd
Kerala Ayurveda Ltd produce medicinali ayurvedici classici, prodotti per il benessere a base di erbe e oggetti di scena...
Kerala Ayurveda Ltd produce medicinali ayurvedici classici, prodotti per il benessere a base di erbe e formulazioni brevettate dal suo stabilimento certificato GMP ad Aluva, Kochi. La gamma di prodotti comprende oli, capsule, compresse, sciroppi e articoli per la cura personale radicati nei testi autentici di Ashtangahridayam. Gli acquirenti all'ingrosso e i distributori internazionali accedono a un catalogo di oltre 800 SKU supportato dalla certificazione OMS-GMP, studi di stabilità e dossier pronti per l'esportazione su misura per la Direttiva europea sulle erbe e le normative statunitensi sugli integratori alimentari.
- Type
- brand seeking distribution
- Location
- Kochi, India
- Founded
- 1945
- Website
- keralaayurveda.biz
- Categories
- Forniture medicali e sanitarie, Skincare e cosmetici
- Markets
- Stati Uniti, Germania, Regno Unito, Emirati Arabi Uniti, Australia
Verified facts
- debarment-clear (green), checked 2026-08-08 OpenSanctions
- corporate-mail-on-domain (green), checked 2026-08-08 Mail server of the company domain
- sanctions-clear (green), checked 2026-08-08 OpenSanctions
- lei-active (green), checked 2026-08-30 GLEIF global LEI register (golden copy)
- export-registered (green), checked 2026-08-21 Pharmexcil member directory (Pharmaceuticals Export Promotion Council of India, Ministry of Commerce)
- registry-activity (green), checked 2026-08-21 Pharmexcil member directory (Pharmaceuticals Export Promotion Council of India, Ministry of Commerce)
- domain-registered (green), checked 2026-08-08 Domain registry record
Claimed certifications
- Good Manufacturing Practice
- ISO 9001, Quality Management IAF CertSearch
- Halal Certified
Import rules for these goods
- Cosmetic products must be notified in the EU Cosmetic Products Notification Portal (CPNP) before being placed on the EU market. European Commission (CPNP)
- For the US market, MoCRA requires cosmetic facility registration and product listing with the FDA. US FDA (MoCRA)
- 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)