NODFORD D-Dimer (CLIA Kit) - Indonesia BPOM Medical Device Registration
NODFORD D-Dimer (CLIA Kit) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20207420070. The device is manufactured by SHENZHEN NODFORD INDUSTRIAL CO., LTD from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is MEDQUEST GLOBAL PARTNERS.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
SHENZHEN NODFORD INDUSTRIAL CO., LTDCountry of Origin
China
Authorized Representative
MEDQUEST GLOBAL PARTNERSAR Address
MENARA SALEMBA LANTAI 7, JALAN SALEMBA RAYA NOMOR 5-5A
Registration Date
Jun 07, 2024
Expiry Date
Oct 25, 2026
Product Type
Haematology Package and Kit
Fibrinogen/fibrin degradation products assay.
Invitro Diagnostics
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