NEUROLITH - Indonesia BPOM Medical Device Registration
NEUROLITH is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21003220011. The device is manufactured by STORZ MEDICAL AG from Switzerland, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. INNOMED JAYA UTAMA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
STORZ MEDICAL AGCountry of Origin
Switzerland
Authorized Representative
PT. INNOMED JAYA UTAMAAR Address
GEDUNG MENARA PALMA LT.5 UNIT #5-03,JL.HR.RASUNA SAID BLOK X2 KAV.6
Registration Date
Mar 21, 2022
Expiry Date
Dec 31, 2023
Product Type
Therapeutic Neurology Equipment
External functional neuromuscular stimulator.
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