REBONSON Gastrointestinal Videoscope - Indonesia BPOM Medical Device Registration
REBONSON Gastrointestinal Videoscope is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20801420343. The device is manufactured by REBONSON INC from Korea, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is GLOBAL MEDICAL PRESS.
This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.
Risk Classification
Product Class
Kelas : 2
Manufacturer
REBONSON INCCountry of Origin
Korea
Authorized Representative
GLOBAL MEDICAL PRESSAR Address
Jl. Raya Kebon Jeruk No.26 RT.011 RW.002, Kelurahan Kebon Jeruk, Kecamatan Kebon Jeruk, Jakarta Barat, DKI Jakarta
Registration Date
Sep 30, 2024
Expiry Date
Jul 26, 2027
Product Type
Diagnostic Gastroenterology-Urology Equipment
Endoscope and accessories
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