VACULAB EDTA K2 - Indonesia BPOM Medical Device Registration
VACULAB EDTA K2 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20209220188. The device is manufactured by ZHEJIANG GONGDONG MEDICAL TECHNOLOGY CO.,LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. INTIGLOBAL PERFECT RESULT SOURCE.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
ZHEJIANG GONGDONG MEDICAL TECHNOLOGY CO.,LTD.Country of Origin
China
Authorized Representative
PT. INTIGLOBAL PERFECT RESULT SOURCEAR Address
KOMPLEK DARMO PARK II BLOK 4/14
Registration Date
Sep 16, 2022
Expiry Date
Sep 15, 2025
Product Type
Products used in the manufacture of blood preparations and preparations of origin and blood
Vacuum-assisted blood collection system.
Invitro Diagnostics
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