GALENUS Malaria P.f./P.v. Rapid Test (Whole Blood) - Indonesia BPOM Medical Device Registration
GALENUS Malaria P.f./P.v. Rapid Test (Whole Blood) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303420395. The device is manufactured by TIANJIN GALENUS MEDICAL CO.,LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is INNOVATION HEALTHCARE INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
TIANJIN GALENUS MEDICAL CO.,LTD.Country of Origin
China
Authorized Representative
INNOVATION HEALTHCARE INDONESIAAR Address
Komplek Ruko Permata Kota, Blok Q No. 11 Jl. Pangeran Tubagus Angke No. 170 Kel. Penjagalan, Kec. Penjaringan, Jakarta Utara 14450
Registration Date
Aug 26, 2024
Expiry Date
Feb 05, 2027
Product Type
Serological Reagents
Plasmodium species antigen detection assays
Invitro Diagnostics
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