NESCO Hemodialysis Dry Powder - Indonesia BPOM Medical Device Registration
NESCO Hemodialysis Dry Powder is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805420042. 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. DJUNIAR & DJUNIAR.
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Risk Classification
Product Class
Kelas : 2
Country of Origin
China
Authorized Representative
PT. DJUNIAR & DJUNIARAR Address
KOMPLEK RUKAN MAHKOTA ANCOL BLOK D NO.26,JLR.E MARTADINATA ,Desa/Kelurahan Pademangan Barat, Kec.Pademangan,Kota Adm.Jakarta Utara, Provinsi DKI Jakarta. Kode Pos:14420
Registration Date
Jan 19, 2024
Expiry Date
Aug 03, 2026
Product Type
Therapeutic Gastroenterology-Urology Equipment
Hemodialysis system and accessories.
Non Electromedic Non Sterile
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TAISHIKANG Haemodialysis Powder B
NESCO Hemodialysis Solution
NESCO Hemodialysis Solution
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