TAISHIKANG Haemodialysis Powder Bi-Cart - Indonesia BPOM Medical Device Registration
TAISHIKANG Haemodialysis Powder Bi-Cart is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805220536. The device is manufactured by TIANJIN TAISHIKANG PHAMACEUTICAL TECHNOLOGY CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is DIAN LANGGENG PRATAMA.
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Risk Classification
Product Class
Kelas : 2
Country of Origin
China
Authorized Representative
DIAN LANGGENG PRATAMAAR Address
Gedung Dinar, Jl. Raden Saleh Raya No. 4 RT.10/RW.01, Kel. Kenari, Kec. Senen. Kota Adm. Jakarta Pusat, Provinsi DKI Jakarta, Kode Pos 10430
Registration Date
Feb 13, 2024
Expiry Date
Dec 31, 2028
Product Type
Therapeutic Gastroenterology-Urology Equipment
Hemodialysis system and accessories.
Non Electromedic Non Sterile
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