Arya Vaidya Sala Kottakkal
Arya Vaidya Sala Kottakkal is a century-old institution manufacturing over 550 classical Ayurvedi…
Arya Vaidya Sala Kottakkal is a century-old institution manufacturing over 550 classical Ayurvedic medicines in WHO-GMP certified facilities. Products include fermented preparations, medicated oils, tablets, granules and external applications derived from authenticated medicinal herbs. Wholesale export partners gain access to the globally recognized Kottakkal brand, comprehensive regulatory documentation packages and dedicated export managers handling compliance for the EU, US, Canada and GCC markets.
- Type
- Manufacturer
- Location
- Malappuram, India
- Founded
- 1902
- Website
- aryavaidyasala.com
- Categories
- Medical & Healthcare Supplies, Skincare & Cosmetics
- Markets
- Germany, United States, United Kingdom, United Arab Emirates, Canada
Verified facts
- domain-registered (green), checked 2026-08-09 Domain registry record
- sanctions-clear (green), checked 2026-08-09 OpenSanctions
- corporate-mail-on-domain (green), checked 2026-08-09 Mail server of the company domain
- debarment-clear (green), checked 2026-08-09 OpenSanctions
- certificate-page-on-site (amber), checked 2026-08-11 Company's own certification page
- standards-mark-certified (green), checked 2026-08-16 EAEU unified register of certificates and declarations
- lei-active (green), checked 2026-08-23 GLEIF global LEI register (golden copy)
Claimed certifications
- Good Manufacturing Practice
- ISO 9001, Quality Management IAF CertSearch
- Halal Certified
- EAC mark (EAEU conformity) EAEU unified register of certificates and declarations
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)