SONOSCAPE Video Duodenoscope - Indonesia BPOM Medical Device Registration
SONOSCAPE Video Duodenoscope is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20801320859. The device is manufactured by SONOSCAPE MEDICAL CORPORATION from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is ENDO INDONESIA.
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
SONOSCAPE MEDICAL CORPORATIONCountry of Origin
China
Authorized Representative
ENDO INDONESIAAR Address
Jl. Raya Menganti 14
Registration Date
Dec 15, 2023
Expiry Date
Dec 31, 2026
Product Type
Diagnostic Gastroenterology-Urology Equipment
Endoscope and accessories
Non Radiation Electromedics
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