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GSI TYMPSTAR PRO Clinical Middle Ear Analyzer - Indonesia BPOM Medical Device Registration

GSI TYMPSTAR PRO Clinical Middle Ear Analyzer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20701612311. The device is manufactured by 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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BPOM Registered
Risk Class Kelas Resiko : B
GSI TYMPSTAR PRO Clinical Middle Ear Analyzer
Analysis ID: AKL 20701612311

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

GRASON-STADLER.

Country of Origin

United States

Authorized Representative

PT. DEMKA SAKTI

AR Address

Jl. Tanah Abang III No. 19 A - B, Jakarta Pusat

Registration Date

Oct 15, 2020

Expiry Date

Jun 25, 2025

Product Type

Diagnostic Ear, Nose and Throat Equipment

Auditory impedance tester.

Non Radiation Electromedics

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