FRAXIS - Indonesia BPOM Medical Device Registration
FRAXIS is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603613393. The device is manufactured by ILOODA CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. ZHENGAN INDONESIA.
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
ILOODA CO., LTD.Country of Origin
Korea
Authorized Representative
PT. ZHENGAN INDONESIAAR Address
Ruko Duren Sawit Center No. 8E, Jl. Raya Duren Sawit
Registration Date
Aug 03, 2020
Expiry Date
May 13, 2025
Product Type
Surgical Equipment
Laser surgical instrument for use in general and plastic surgery and in dermatology.
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