SPHERA DUO Hydrocephalus Shunt System High Pressure - Indonesia BPOM Medical Device Registration
SPHERA DUO Hydrocephalus Shunt System High Pressure is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21003910723. The device is manufactured by HP BIOPROTESES LTDA. from Brazil, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. KHALIFI SHINES DJAYA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
HP BIOPROTESES LTDA.Country of Origin
Brazil
Authorized Representative
PT. KHALIFI SHINES DJAYAAR Address
Ruko Ayodhya Blok G Nomor : 23 Jalan MH. Thamrin Nomor : 17, Kel. Kelapa Indah, Kec. Tangerang, Kota Tangerang, Banten 15117
Registration Date
May 13, 2024
Expiry Date
Nov 07, 2027
Product Type
Therapeutic Neurology Equipment
Central nervous system fluid shunt and components.
Non Electromedic Sterile
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