NODFORD HbA1c Test Kit (Dry Fluorescence Immunoassay) - Indonesia BPOM Medical Device Registration

NODFORD HbA1c Test Kit (Dry Fluorescence Immunoassay) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20207420137. The device is manufactured by SHENZHEN NODFORD INDUSTRIAL CO., LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MULTISERA INDOSA.

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BPOM Registered

Risk Class Kelas Resiko : B

NODFORD HbA1c Test Kit (Dry Fluorescence Immunoassay)

Analysis ID: AKL 20207420137

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

SHENZHEN NODFORD INDUSTRIAL CO., LTD

Country of Origin

China

Authorized Representative

PT. MULTISERA INDOSA

AR Address

Jl. Jend. Sudirman No. 689 RT/RW : 21/07

Registration Date

Aug 31, 2024

Expiry Date

Nov 09, 2026

Product Type

Haematology Package and Kit

Glycosylated hemoglobin assay.

Invitro Diagnostics

DJ Fang

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Kelas Resiko : A

NODFORD HbA1c Test Kit (Dry Fluorescence Immunoassay) - 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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