Kerala Ayurveda Ltd
Kerala Ayurveda Ltd fabrica medicinas ayurvédicas clásicas, productos a base de hierbas para el bienestar y prop…
Kerala Ayurveda Ltd fabrica medicinas ayurvédicas clásicas, productos de bienestar a base de hierbas y formulaciones patentadas en su planta con certificación GMP en Aluva, Kochi. La gama de productos abarca aceites, cápsulas, tabletas, jarabes y artículos de cuidado personal basados en textos auténticos de Ashtangahridayam. Los compradores mayoristas y distribuidores internacionales acceden a un catálogo de más de 800 SKU respaldado por la certificación WHO-GMP, estudios de estabilidad y expedientes listos para la exportación adaptados a la Directiva herbaria europea y las regulaciones de suplementos dietéticos de EE. UU.
- Type
- brand seeking distribution
- Location
- Kochi, India
- Founded
- 1945
- Website
- keralaayurveda.biz
- Categories
- Suministros médicos y sanitarios, Cuidado de la piel y cosmética
- Markets
- Estados Unidos, Alemania, Reino Unido, Emiratos Árabes Unidos, 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)