REBORN Zebra Guidewire - Indonesia BPOM Medical Device Registration
REBORN Zebra Guidewire is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805220402. The device is manufactured by HUNAN REBORN MEDICAL SCIENCE AND TECHNOLOGY DEVELOPMENT CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. PARAMA TRIPTA MERCURY.
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Risk Classification
Product Class
Kelas : 2
Country of Origin
China
Authorized Representative
PT. PARAMA TRIPTA MERCURYAR Address
Jalan Terusan Prof. Dr. Ir. Sutami kavling 3, Desa/Kelurahan Sarijadi, Kec.Sukasari, Kota Bandung, Provinsi Jawa Barat, Kode Pos: 40151
Registration Date
Nov 06, 2022
Expiry Date
May 04, 2027
Product Type
Therapeutic Gastroenterology-Urology Equipment
Urological catheter and accessories.
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