MKCELLS Bicarbonate B - Indonesia BPOM Medical Device Registration
MKCELLS Bicarbonate B is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805420488. The device is manufactured by TIANJIN TAISHIKANG PHARMACEUTICAL TECHNOLOGY CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. INTERSKALA SEHAT SEJAHTERA.
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MKCELLS Bicarbonat B
Risk Classification
Product Class
Kelas : 2
Country of Origin
China
Authorized Representative
PT. INTERSKALA SEHAT SEJAHTERAAR Address
Green Sedayu Bizpark, Blok DM.015/116, Jl. Daan Mogot KM.18 RT 03 RW 08
Registration Date
Sep 19, 2024
Expiry Date
Sep 18, 2027
Product Type
Therapeutic Gastroenterology-Urology Equipment
Hemodialysis system and accessories.
Non Electromedic Sterile
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