DEMAX Manifolds - Indonesia BPOM Medical Device Registration
DEMAX Manifolds is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20504413193. 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
Jan 01, 2021
Expiry Date
Nov 09, 2025
Product Type
Surgical Cardiology Equipment
Cardiopulmonary bypass adaptor, stopcock, manifold, or fitting.
Non Electromedic Sterile
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