DEMAX Guiding Catheter - Indonesia BPOM Medical Device Registration
DEMAX Guiding Catheter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501420426. The device is manufactured by TIANJIN DEMAX MEDICAL TECHNOLOGY CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PURE SOUTHEAST ASIA INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
TIANJIN DEMAX MEDICAL TECHNOLOGY CO., LTD.Country of Origin
China
Authorized Representative
PURE SOUTHEAST ASIA INDONESIAAR Address
Equity Tower, 26th Floor H, Kav 52-53, Jl. Jenderal Sudirman
Registration Date
Aug 07, 2024
Expiry Date
Mar 21, 2029
Product Type
Diagnostic Cardiology Equipment
Percutaneous catheter.
Non Electromedic Sterile
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