SINOCARE β 2-Microglobulin / Cystatin C Reagent Kit - Indonesia BPOM Medical Device Registration

SINOCARE β 2-Microglobulin / Cystatin C Reagent Kit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101124024. The device is manufactured by CHANGSHA SINOCARE INC. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is SINOCARE HEALTHCARE INDONESIA.

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BPOM Registered

Risk Class Kelas Resiko : C

SINOCARE β 2-Microglobulin / Cystatin C Reagent Kit

Analysis ID: AKL 20101124024

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

CHANGSHA SINOCARE INC.

Country of Origin

China

Authorized Representative

SINOCARE HEALTHCARE INDONESIA

AR Address

Equity Tower Lantai 37, SCBD, Jl.Jend. Sudirman Kav.52-53

Registration Date

Nov 23, 2023

Expiry Date

Sep 13, 2026

Product Type

Clinical Chemistry Test System

Multi parameter clinical chemistry test system

Invitro Diagnostics

DJ Fang

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Other Products from CHANGSHA SINOCARE INC.

Products from the same manufacturer (10 products)

CHANGSHA SINOCARE INC.

Kelas Resiko : B

SINOCARE β 2-Microglobulin / Cystatin C Reagent Kit - 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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