GSI AudioStar Pro Clinical Audiometer - Indonesia BPOM Medical Device Registration
GSI AudioStar Pro Clinical Audiometer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20701714544. The device is manufactured by DIAGNOSTIC GROUP LLC - DBA GRASON-STADLER from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. DEMKA SAKTI.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
DIAGNOSTIC GROUP LLC - DBA GRASON-STADLERCountry of Origin
United States
Authorized Representative
PT. DEMKA SAKTIAR Address
Jl. Tanah Abang III No. 19 A - B, Jakarta Pusat
Registration Date
Jul 09, 2021
Expiry Date
Nov 07, 2025
Product Type
Diagnostic Ear, Nose and Throat Equipment
Audiometer.
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