RENACARE AV Fistula Needle Sets - Indonesia BPOM Medical Device Registration
RENACARE AV Fistula Needle Sets is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805220392. The device is manufactured by SHANDONG WEIGAO BLOOD PURIFICATION PRODUCTS CO.,LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. RENALMED TIARA MAIN.
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Risk Classification
Product Class
Kelas : 2
Country of Origin
China
Authorized Representative
PT. RENALMED TIARA MAINAR Address
Gedung Enseval Lantai 2 Jl. Pulo Lentut No. 10 Kawasan Industri Pulogadung, Jakarta Timur Tlp. 021-4618330
Registration Date
Oct 27, 2022
Expiry Date
Jul 28, 2025
Product Type
Therapeutic Gastroenterology-Urology Equipment
Hemodialysis system and accessories.
Non Electromedic Sterile
RENACARE A.V Fistula Needle Set
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SAFIL MEDICAL PRODUCTS INTERNATIONAL TRANSPORT INDUSTRY AND TRADE CO., LTD.,
RENMED AV FISTULA
SHANDONG WEIGAO BLOOD PURIFICATION PRODUCTS CO.,LTD.

