MLH A.V. Fistula Needle Set - Indonesia BPOM Medical Device Registration
MLH A.V. Fistula Needle Set is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805024940. The device is manufactured by JIANGXI SANXIN MEDTECH CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is LESTARI HUSADA DOUGH.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
JIANGXI SANXIN MEDTECH CO., LTD.Country of Origin
China
Authorized Representative
LESTARI HUSADA DOUGHAR Address
Jl. Kartini VIII Nomor 11
Registration Date
Aug 01, 2023
Expiry Date
May 15, 2028
Product Type
Therapeutic Gastroenterology-Urology Equipment
Hemodialysis system and accessories.
Non Electromedic Sterile

