DEMAX Interventional Device Set - Indonesia BPOM Medical Device Registration
DEMAX Interventional Device Set is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501021780. The device is manufactured by BEIJING DEMAX MEDICAL TECHNOLOGY CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. GIRI SAKTI UTAMA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
BEIJING DEMAX MEDICAL TECHNOLOGY CO., LTD.Country of Origin
China
Authorized Representative
PT. GIRI SAKTI UTAMAAR Address
Komp. Girimekar Permai Blok D No. 15 RT. 03 RW. 21 Desa Giri Mekar Kec. Cilengkrang
Registration Date
Apr 07, 2020
Expiry Date
Dec 26, 2024
Product Type
Diagnostic Cardiology Equipment
Syringe actuator for an injector.
Non Electromedic Sterile
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