AKREOS Single Use Insertion Device - Indonesia BPOM Medical Device Registration
AKREOS Single Use Insertion Device is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11203916579. The device is manufactured by BAUSCH & LOMB INC. from United States, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. GLOBAL ALIGNED MEDIKA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
BAUSCH & LOMB INC.Country of Origin
United States
Authorized Representative
PT. GLOBAL ALIGNED MEDIKAAR Address
RUKO PULOGADUNG TRADE CENTRE (PTC) BLOK 8-A NO.7 JL.RAYA BEKASI KM.21 RT.003 RW.003 RAWA TERATE,CAKUNG,JAKARTA TIMUR
Registration Date
Mar 28, 2023
Expiry Date
Feb 21, 2028
Product Type
Surgical Eye Equipment
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