SHOCKPULSE-SE Lithotripsy System - Indonesia BPOM Medical Device Registration
SHOCKPULSE-SE Lithotripsy System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20804026567. The device is manufactured by GYRUS ACMI, INC. from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. MURSMEDIC.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
GYRUS ACMI, INC.Country of Origin
United States
Authorized Representative
PT. MURSMEDICAR Address
Jl. Bukit Gading Raya, Komplek Gading Bukit Indah Blok SA No. 6, Kelurahan Kelapa Gading Barat
Registration Date
Mar 16, 2023
Expiry Date
Mar 31, 2025
Product Type
Gastroenterology-Surgical Urology Equipment
Electrohydraulic lithotriptor.
Non Radiation Electromedics
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