SANKRINA Hollow Fiber Dialyzer (PF Series) - Indonesia BPOM Medical Device Registration
SANKRINA Hollow Fiber Dialyzer (PF Series) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805320990. The device is manufactured by BAIN MEDICAL EQUIPMENT (GUANGZHOU) CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. KARYATAMA MANDIRI BUSINESS.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
BAIN MEDICAL EQUIPMENT (GUANGZHOU) CO., LTD.Country of Origin
China
Authorized Representative
PT. KARYATAMA MANDIRI BUSINESSAR Address
Komplek Ruko D\'Best Blok B No. 39 Jl. RS Fatmawati No. 15 Gandaria Selatan
Registration Date
Mar 27, 2024
Expiry Date
Nov 01, 2026
Product Type
Therapeutic Gastroenterology-Urology Equipment
Hemodialysis system and accessories.
Non Electromedic Sterile
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SANKRINA Hollow Fiber Dialyzer (H Series)
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SANKRINA Hollow Fiber Dialyzer (P Series)
BAIN MEDICAL EQUIPMENT (GUANGZHOU) CO., LTD.
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