FLOW-i C20 Anesthesia System - Indonesia BPOM Medical Device Registration
FLOW-i C20 Anesthesia System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403113452. The device is manufactured by MAQUET CRITICAL CARE AB. from Sweden, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. INDOSOPHA SAKTI.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
MAQUET CRITICAL CARE AB.Country of Origin
Sweden
Authorized Representative
PT. INDOSOPHA SAKTIAR Address
JL. MAMPANG PRAPATAN RAYA NO.1
Registration Date
Dec 23, 2024
Expiry Date
Dec 31, 2025
Product Type
Therapeutic Anesthesia Equipment
Gas machine for anesthesia or analgesia.
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