HLL Lifecare
Empresa del gobierno de la India, productos sanitarios que llegan hasta la última milla.
HLL Lifecare (Hindustan Latex Limited) es una empresa Mini-Ratna del gobierno de la India con sede en Thiruvananthapuram, que fabrica anticonceptivos, guantes quirúrgicos, condones, DIU, toallas sanitarias y productos de diagnóstico. Abastece a programas nacionales de salud y exporta a más de 130 países de África, Asia y Medio Oriente.
- Type
- brand seeking distribution
- Location
- Thiruvananthapuram, India
- Founded
- 1966
- Website
- lifecarehll.com
- Categories
- Suministros médicos y sanitarios, Cuidado personal
- Markets
- India, Emiratos Árabes Unidos, Nigeria, Kenia, Bangladés
Verified facts
- corporate-mail-on-domain (green), checked 2026-08-08 Mail server of the company domain
- domain-registered (green), checked 2026-08-08 Domain registry record
- fda-registered (green), checked 2026-08-08 FDA
- debarment-clear (green), checked 2026-08-08 OpenSanctions
- sanctions-clear (green), checked 2026-08-08 OpenSanctions
- standards-mark-certified (green), checked 2026-08-21 Bureau of Indian Standards (BIS), all-India first licence report (ISI Standard Mark)
- export-registered (green), checked 2026-08-21 Pharmexcil member directory (Pharmaceuticals Export Promotion Council of India, Ministry of Commerce)
- lei-active (green), checked 2026-08-30 GLEIF global LEI register (golden copy)
- registry-activity (green), checked 2026-08-21 Pharmexcil member directory (Pharmaceuticals Export Promotion Council of India, Ministry of Commerce)
Claimed certifications
- Good Manufacturing Practice
- ISO 9001, Quality Management IAF CertSearch
- ISO 13485, Medical Devices Quality IAF CertSearch
- FDA Registered FDA Establishment Registration
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)