DEMAX Balloon In-Deflation Device - Indonesia BPOM Medical Device Registration
DEMAX Balloon In-Deflation Device is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501413744. 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 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
GIRI SAKTI UTAMAAR Address
Komp. Girimekar Permai Blok D No. 15 RT. 03 RW. 21 Desa Giri Mekar Kec. Cilengkrang
Registration Date
Dec 29, 2020
Expiry Date
Nov 09, 2025
Product Type
Diagnostic Cardiology Equipment
Angiographic injector and syringe.
Non Electromedic Sterile
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