WONDFO AFP (CLIA) - Indonesia BPOM Medical Device Registration
WONDFO AFP (CLIA) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20306420123. The device is manufactured by SHENZEN TISENC MEDICAL DEVICES CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is ZOE PELITA NUSANTARA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
SHENZEN TISENC MEDICAL DEVICES CO., LTD.Country of Origin
China
Authorized Representative
ZOE PELITA NUSANTARAAR Address
JALAN CIKINI II NO 8 B
Registration Date
Jul 31, 2024
Expiry Date
Aug 01, 2028
Product Type
Tumor Antigen Immunologic Test System
AFP-L3% immunological test system.
Invitro Diagnostics
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WONDFO LH (CLIA)
WONDFO Free Triiodothyronine (CLIA)
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WONDFO CA19-9 (CLIA)
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