APOLLO Single Use High Pressure - Indonesia BPOM Medical Device Registration
APOLLO Single Use High Pressure is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501910509. The device is manufactured by SICHUAN GUANGYUAN KANGKANG MEDICAL INSTRUMENT CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MURTI INDAH SENTOSA.
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Risk Classification
Product Class
Kelas : 2
Country of Origin
China
Authorized Representative
PT. MURTI INDAH SENTOSAAR Address
WISMA MURTI JL. SULTAN ISKANDAR MUDA KAV. 29 ARTERI PONDOK INDAH
Registration Date
Apr 24, 2022
Expiry Date
Dec 31, 2026
Product Type
Diagnostic Cardiology Equipment
Angiographic Injector and Syringe
Non Electromedic Sterile
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