PURIFIER H160 High Flux Dialyser - Indonesia BPOM Medical Device Registration
PURIFIER H160 High Flux Dialyser is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805123322. The device is manufactured by SAFIL TIBBI URUNLERI ULUSLARARASI NAKLIYAT SANAYI VE TICARET A.S. 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
Jun 19, 2023
Expiry Date
Jun 12, 2028
Product Type
Therapeutic Gastroenterology-Urology Equipment
Hemodialysis system and accessories.
Non Electromedic Sterile
