COMFORT-IN ™ Derma - Indonesia BPOM Medical Device Registration
COMFORT-IN ™ Derma is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902420026. The device is manufactured by MIKA MEDICAL CO from Korea, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. FIRST MEDIKACITRA CENTER.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
MIKA MEDICAL COCountry of Origin
Korea
Authorized Representative
PT. FIRST MEDIKACITRA CENTERAR Address
JL. PASEBAN RAYA NO.21
Registration Date
Jan 08, 2024
Expiry Date
Sep 22, 2025
Product Type
Therapeutic General and Individual Hospital Equipment
Nonelectrically powered fluid injector.
Non Electromedic Sterile
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