FARCATH Triple Lumen Haemodialysis Catheter Kit - Indonesia BPOM Medical Device Registration
FARCATH Triple Lumen Haemodialysis Catheter Kit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805028295. 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. DIAN LANGGENG PRATAMA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
GUANGDONG BAIHE MEDICAL TECHNOLOGY CO., LTD.Country of Origin
China
Authorized Representative
PT. DIAN LANGGENG PRATAMAAR Address
Jl. Raden Saleh Raya No. 4
Registration Date
Dec 30, 2020
Expiry Date
Dec 30, 2023
Product Type
Therapeutic Gastroenterology-Urology Equipment
Blood access device and accessories.
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