PURIFIER L180 Low Flux Dialyser - Indonesia BPOM Medical Device Registration
PURIFIER L180 Low Flux Dialyser is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805220130. The device is manufactured by SAFIL MEDICAL PRODUCTS INTERNATIONAL TRANSPORT INDUSTRY AND TRADE CO., LTD., from Turkey, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is RENALMED TIARA MAIN.
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Risk Classification
Product Class
Kelas : 2
Country of Origin
Turkey
Authorized Representative
RENALMED TIARA MAINAR Address
Gedung Enseval Lantai 2 Jl. Pulo Lentut No. 10 Kawasan Industri Pulogadung, Jakarta Timur Tlp. 021-4618330
Registration Date
May 16, 2022
Expiry Date
Jul 13, 2026
Product Type
Therapeutic Gastroenterology-Urology Equipment
Hemodialysis system and accessories.
Non Electromedic Sterile

