TOSOH ST AIA-PACK CA 125 - Indonesia BPOM Medical Device Registration
TOSOH ST AIA-PACK CA 125 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20306113283. The device is manufactured by TOSOH AIA. from Japan, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. KARINDO ALKESTRON.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
TOSOH AIA.Country of Origin
Japan
Authorized Representative
PT. KARINDO ALKESTRONAR Address
JL. TOMANG RAYA NO.17
Registration Date
Nov 11, 2021
Expiry Date
Aug 31, 2026
Product Type
Tumor Antigen Immunologic Test System
Tumor-associated antigen immunological test system.
Invitro Diagnostics
TOSOH AIA-PACK HBsAb Calibrator Set
TOSOH AIA-PACK IgE II Calibrator Set
TOSOH AIA-PACK CA 19-9 Calibrator Set
TOSOH AIA-PACK CA 15-3 Calibrator Set
TOSOH ST AIA-PACK CA 19-9
TOSOH ST AIA-PACK CA 15-3
TOSOH ST AIA-CEA PACK
TOSOH AIA-PACK AFP Calibrator Set
TOSOH AIA - PACK CEA Calibrator Set
TOSOH ST AIA-PACK AFP
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TOSOH AIA-PACK HBV Antibody Control Set
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LABOTRON Microplate Reader LB-6200
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TOSOH ST AIA-PACK cTnI 3rd Gen Calibrator Set
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TOSOH ST AIA-PACK Myoglobin Calibrator Set
TOSOH AIA INC.
TOSOH ST AIA-PACK HBeAb
TOSOH AIA INC.
TOSOH ST AIA-PACK HBeAg
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TOSOH ST AIA-PACK Intact PTH SAMPLE DILUTING SOLUTION
TOSOH AIA INC.
TOSOH ST AIA-PACK Myoglobin
TOSOH AIA INC.