DIAMOND Buffer Pack - Indonesia BPOM Medical Device Registration
DIAMOND Buffer Pack is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101818697. 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 INDOMEDIKA DUTA MANDIRI.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
DIAMOND DIAGNOSTICS, INC.Country of Origin
United States
Authorized Representative
INDOMEDIKA DUTA MANDIRIAR Address
RUKO TAMAN JUANDA BLOK B1 No. 6 RT. 008 RW. 004, KELURAHAN DUREN JAYA
Registration Date
Nov 02, 2021
Expiry Date
Jun 01, 2024
Product Type
Clinical Chemistry Test System
Calibrator (cair)
Invitro Diagnostics
