LILY Laryngeal Mask Airway - Indonesia BPOM Medical Device Registration
LILY Laryngeal Mask Airway is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403220032. The device is manufactured by BENQ MEDICAL TECHNOLOGY CORPORATION TAICHUNG FACTORY from Taiwan (China), and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is INDOMEDIKA SOLUSINDO.
This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.
Risk Classification
Product Class
Kelas : 2
Country of Origin
Taiwan (China)
Authorized Representative
INDOMEDIKA SOLUSINDOAR Address
GRIYA KAYU PUTIH I Jl. Kayu Mas Raya No. 1/Q Kelurahan Pulogadung Kecamatan Pulogadung
Registration Date
Jan 17, 2022
Expiry Date
Aug 31, 2024
Product Type
Therapeutic Anesthesia Equipment
Oropharyngeal airway.
Non Electromedic Sterile
INDOMEDIPRO Breathing Circuit System
FOREMOUNT ENTERPRISE CO., LTD. (MINZU FACTORY)
TUOREN Connecting Tube
HENAN TUOREN BEST MEDICAL DEVICE CO., LTD.
FRESH Oxygen Mask
HENAN TUOREN BEST MEDICAL DEVICE CO., LTD.
LILY Free Trachea Closed Suction Catheter
LILY MEDICAL CORPORATION
INDOMEDIPRO Collapsible Breathing System
FOREMOUNT ENTERPRISE CO., LTD. (MINZU FACTORY)
INDOMEDIPRO Catheter Mounts
FOREMOUNT ENTERPRISE CO., LTD.
INDOMEDIPRO Nebulizer Kit and Accessories
HEADSTAR MEDICAL PRODUCTS CO., LTD.

