BDI Lab Fluid Pack - Indonesia BPOM Medical Device Registration
BDI Lab Fluid Pack is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101220161. The device is manufactured by DIAMOND DIAGNOSTICS, INC. from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. BERLIANTAMA DIAGNOSTIKA INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
DIAMOND DIAGNOSTICS, INC.Country of Origin
United States
Authorized Representative
PT. BERLIANTAMA DIAGNOSTIKA INDONESIAAR Address
JL.TAMAN SUNTER INDAH BLOK HJ2 NO.16
Registration Date
Feb 09, 2022
Expiry Date
Feb 07, 2025
Product Type
Clinical Chemistry Test System
Calibrator (cair)
Invitro Diagnostics
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