GIGASEPT PAA - Indonesia BPOM Medical Device Registration
GIGASEPT PAA is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20903710333. The device is manufactured by BIOXAL Ltd. from France, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. DEMKA SAKTI.
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
BIOXAL Ltd.Country of Origin
France
Authorized Representative
PT. DEMKA SAKTIAR Address
Jl. Tanah Abang III No. 19 A - B, Jakarta Pusat
Registration Date
Oct 05, 2023
Expiry Date
Jul 11, 2028
Product Type
General Hospital Equipment and Other Individuals
Liquid chemical sterilants/high level disinfectants.
Non Electromedic Non Sterile
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