URUS ™ Single-Use Digital Flexible Ureteroscope - Indonesia BPOM Medical Device Registration
URUS ™ Single-Use Digital Flexible Ureteroscope is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20801420041. The device is manufactured by DYNE MEDICAL GROUP INC from Korea, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. KIRANA JAYA LESTARI.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
DYNE MEDICAL GROUP INCCountry of Origin
Korea
Authorized Representative
PT. KIRANA JAYA LESTARIAR Address
Jl. Tanah Abang II No. 37 RT.001/RW.003, Kode Pos 10160, Kel. Petojo Selatan, Kec. Gambir, Kota Jakarta Pusat, Provinsi DKI Jakarta
Registration Date
Feb 01, 2024
Expiry Date
Nov 20, 2026
Product Type
Diagnostic Gastroenterology-Urology Equipment
Endoscope and accessories.
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