iSIA C-reactive protein (CRP+hs-CRP) Rapid Test Kit (QDs Immunofluorescence Method) - Indonesia BPOM Medical Device Registration

iSIA C-reactive protein (CRP+hs-CRP) Rapid Test Kit (QDs Immunofluorescence Method) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20305321041. The device is manufactured by CHONGQING ISIA BIO-TECHNOLOGY CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. HEALTHY FAMILY FOCUS.

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BPOM Registered

Risk Class Kelas Resiko : B

iSIA C-reactive protein (CRP+hs-CRP) Rapid Test Kit (QDs Immunofluorescence Method)

Analysis ID: AKL 20305321041

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

CHONGQING ISIA BIO-TECHNOLOGY CO., LTD.

Country of Origin

China

Authorized Representative

PT. HEALTHY FAMILY FOCUS

AR Address

Komplek Delta Building Blok B 1-2, Jalan Suryopranoto No. 1-9, Prov. DKI Jakarta, Kota Jakarta Pusat, Kec. Gambir, Kel. Petojo Selatan

Registration Date

Aug 28, 2023

Expiry Date

May 05, 2028

Product Type

Immunological Test System

C-reactive protein immunological test system.

Invitro Diagnostics

DJ Fang

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iSIA C-reactive protein (CRP+hs-CRP) Rapid Test Kit (QDs Immunofluorescence Method) - Indonesia BPOM Medical Device Registration

Risk Classification

Product Class

Manufacturer

Country of Origin

Authorized Representative

AR Address

Registration Date

Expiry Date

Product Type

DJ Fang

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