SRI Disposable Fistula Needles - Indonesia BPOM Medical Device Registration
SRI Disposable Fistula Needles is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805420371. The device is manufactured by GUANGDONG BAIHE MEDICAL TECHNOLOGY CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. RENAL FACILITIES INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
GUANGDONG BAIHE MEDICAL TECHNOLOGY CO., LTD.Country of Origin
China
Authorized Representative
PT. RENAL FACILITIES INDONESIAAR Address
KOMP. GOLDEN BOULEVARD BLOK G2 / 39 RT.04 RW.010
Registration Date
Jul 05, 2024
Expiry Date
Jul 03, 2027
Product Type
Therapeutic Gastroenterology-Urology Equipment
Hemodialysis system and accessories.
Non Electromedic Sterile
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