REXTON Arena HP3 - Indonesia BPOM Medical Device Registration
REXTON Arena HP3 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20702320141. The device is manufactured by SIVANTOS PTE LTD from Singapore, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. GANTAPI BOJONG ABADI.
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
Manufacturer
SIVANTOS PTE LTDCountry of Origin
Singapore
Authorized Representative
PT. GANTAPI BOJONG ABADIAR Address
JL. Raya Serpong KM. 8 Blok A No. 1, Komplek Puri Mutiara Serpong
Registration Date
Jun 27, 2023
Expiry Date
Jan 31, 2028
Product Type
Prosthetic Ear, Nose and Throat Equipment
(Deleted) Hearing Aid
Non Radiation Electromedics

