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.
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
GRASON-STADLER.Country of Origin
United States
Authorized Representative
PT. DEMKA SAKTIAR 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
DIRECTCHECK Whole Blood Controls
ACCRIVA DIAGNOSTICS, INC.
ADVANCED Insufflation Filter with Tubing Set
ADVANCED MEDICAL DESIGN.,CO. LTD
HEMOCHRON PT Cuvettes
ACCRIVA DIAGNOSTICS INC.
HEMOCHRON ACT+ Cuvettes
ACCRIVA DIAGNOSTICS INC.
Vyntus Pneumo
VYAIRE MEDICAL GMBH
BRUMABA CL-GENIUS Operating Table
BRUMABA GMBH & CO. KG.
MEDIHONEY Antibacterial Wound Gel Dressing
DERMA SCIENCES,INC
MEDIHONEY Paste
DERMA SCIENCES INC.
MEDIHONEY HCS-Hydrogel Colloidal Sheet with Antibacterial Honey
DERMA SCIENCES, INC.
ALTUS Operating Lamp
ST FRANCIS MEDICAL EQUIPMENT CO., LTD

