DIACAN PRO Fistula Needle - Indonesia BPOM Medical Device Registration
DIACAN PRO Fistula Needle is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805810014. 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. B. BRAUN MEDICAL INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
NIPRO (THAILAND) CORPORATION LIMITEDCountry of Origin
Thailand
Authorized Representative
PT. B. BRAUN MEDICAL INDONESIAAR Address
Gedung Tempo Scan Tower Lantai 30, Jl. HR Rasuna Said Kav. 3-4 RT 009 RW 004 Kel. Kuningan Timur, Kec. Setiabudi, Kota Administrasi Jakarta Selatan
Registration Date
Dec 07, 2021
Expiry Date
Sep 08, 2026
Product Type
Therapeutic Gastroenterology-Urology Equipment
Blood access device and accessories.
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