CDI Rapid M-Amp Screen - Indonesia BPOM Medical Device Registration
CDI Rapid M-Amp Screen is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20103320588. The device is manufactured by CAL-TECH DIAGNOSTIC INC. from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is MAIN ONCOPROBE.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
CAL-TECH DIAGNOSTIC INC.Country of Origin
United States
Authorized Representative
MAIN ONCOPROBEAR Address
APRT.ISTANA HARMONI LT.DASAR UNIT 1M, KOMP.HARMONI PLAZA JL.SURYOPRANOTO NO.2, PETOJO UTARA
Registration Date
Nov 06, 2023
Expiry Date
Jun 02, 2027
Product Type
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