MAGLUMI EPO (CLIA) - Indonesia BPOM Medical Device Registration

MAGLUMI EPO (CLIA) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20207520012. The device is manufactured by SHENZHEN NEW INDUSTRIES BIOMEDICAL ENGINEERING CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. SNIBE DIAGNOSTIC INDONESIA.

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BPOM Registered

Risk Class Kelas Resiko : B

MAGLUMI EPO (CLIA)

Analysis ID: AKL 20207520012

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

SHENZHEN NEW INDUSTRIES BIOMEDICAL ENGINEERING CO., LTD.

Country of Origin

China

Authorized Representative

PT. SNIBE DIAGNOSTIC INDONESIA

AR Address

TEMPO SCAN TOWER, LANTAI 21, JALAN H.R. RASUNA SAID KAV. 3-4

Registration Date

Feb 03, 2025

Expiry Date

Aug 13, 2029

Product Type

Haematology Package and Kit

Erythropoietin assay.

Invitro Diagnostics

DJ Fang

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MAGLUMI EPO (CLIA) - Indonesia BPOM Medical Device Registration

Risk Classification

Product Class

Manufacturer

Country of Origin

Authorized Representative

AR Address

Registration Date

Expiry Date

Product Type

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