NEW GP Blood Collection Tubes EDTA K2 - Indonesia BPOM Medical Device Registration
NEW GP Blood Collection Tubes EDTA K2 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101221339. 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. GOLDEN PRATAMA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
ZHEJIANG GONGDONG MEDICAL TECHNOLOGY CO., LTD.Country of Origin
China
Authorized Representative
PT. GOLDEN PRATAMAAR Address
Puri Metropolitan Blok F7/12B, Petir, Cipondoh, Tangerang, Banten
Registration Date
Aug 23, 2022
Expiry Date
Aug 23, 2025
Product Type
Clinical Chemistry Test System
Blood specimen collection device
Invitro Diagnostics
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