BAXTER AV Fistula Needles - Indonesia BPOM Medical Device Registration
BAXTER AV Fistula Needles is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805020034. The device is manufactured by NIPRO (THAILAND) CORPORATION LIMITED from Thailand, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. TAWADA HEALTHCARE.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
NIPRO (THAILAND) CORPORATION LIMITEDCountry of Origin
Thailand
Authorized Representative
PT. TAWADA HEALTHCAREAR Address
Rukan Permata Senayan Blok A18-19 Lantai 5 Jl. Tentara Pelajar No. 5
Registration Date
Jul 09, 2024
Expiry Date
Dec 31, 2025
Product Type
Therapeutic Gastroenterology-Urology Equipment
Blood access device and accessories.
Non Electromedic Sterile
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VACUETTE Safety Blood Collection Set + Luer Adapter
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DIACAN Buttonhole
DIACAN Safety
DIACAN PRO Fistula Needle
NIPRO Hypodermic Needle
NIPRO Arterial Venous Fistula Needles
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