BDI Lab Vacuum Tube EDTA K3 PET - Indonesia BPOM Medical Device Registration
BDI Lab Vacuum Tube EDTA K3 PET is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101322998. The device is manufactured by JIANGSU KANGJIAN MEDICAL APPARATUS CO., LTD. from China, 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
JIANGSU KANGJIAN MEDICAL APPARATUS CO., LTD.Country of Origin
China
Authorized Representative
PT. BERLIANTAMA DIAGNOSTIKA INDONESIAAR Address
JL.TAMAN SUNTER INDAH BLOK HJ2 NO.16
Registration Date
Apr 28, 2023
Expiry Date
Apr 28, 2026
Product Type
Clinical Chemistry Test System
Blood specimen collection device
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