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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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BPOM Registered
Risk Class Kelas Resiko : B
GALENUS Malaria P.f./P.v. Rapid Test (Whole Blood)
Analysis ID: AKL 20303420395

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

INNOVATION HEALTHCARE INDONESIA

AR 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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