BODITECH Tn-I Plus Control - Indonesia BPOM Medical Device Registration
BODITECH Tn-I Plus Control is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101520060. The device is manufactured by BODITECH MED INC., from Korea, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. BODITECH MED INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
BODITECH MED INC.,Country of Origin
Korea
Authorized Representative
PT. BODITECH MED INDONESIAAR Address
Ruko Alam Sutera, Jalur Sutera Kavling 25 B-C No.1
Registration Date
Jan 09, 2025
Expiry Date
Feb 05, 2029
Product Type
Clinical Chemistry Test System
Quality control material (assayed and unassayed) (cair)
Invitro Diagnostics
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AFIAS PSA
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AFIAS CRP
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AFIAS TSH
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BODITECH MED INC.,