COSMOS - Indonesia BPOM Medical Device Registration
COSMOS is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501125848. The device is manufactured by ECHONOUS, INC. from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. TRITRA PRIMA INDONESIA.
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KOSMOS
Risk Classification
Product Class
Kelas : 2
Manufacturer
ECHONOUS, INC.Country of Origin
United States
Authorized Representative
PT. TRITRA PRIMA INDONESIAAR Address
Taman Sari Persada Blok F-1 Nomor 10
Registration Date
Oct 12, 2021
Expiry Date
Dec 31, 2025
Product Type
Diagnostic Radiology Equipment
Ultrasonic pulsed doppler imaging system.
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