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 20902910776. 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
Dec 17, 2024
Expiry Date
Dec 31, 2026
Product Type
Therapeutic General and Individual Hospital Equipment
Piston syringe.
Non Electromedic Sterile
APOLLO Single Use High Pressure
SICHUAN GUANGYUAN KANGKANG MEDICAL INSTRUMENT CO., LTD.
APOLLO Single Use High Pressure
SICHUAN GUANGYUAN KANGKANG MEDICAL INSTRUMENT CO., LTD
APOLLO Single Use High Pressure
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