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Giesse_Hematology Analyzer Diluent GS3 - Indonesia BPOM Medical Device Registration

Giesse_Hematology Analyzer Diluent GS3 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20208220139. The device is manufactured by GIESSE DIAGNOSTICS. from Italy, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is DUAL NOBLE LIGHT.

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BPOM Registered
Risk Class Kelas Resiko : B
Giesse_Hematology Analyzer Diluent GS3
Analysis ID: AKL 20208220139

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Italy

Authorized Representative

DUAL NOBLE LIGHT

AR Address

Ruko Villa Jatibening Toll Blok A no. 2 Jatibening - Bekasi

Registration Date

Jun 28, 2022

Expiry Date

Oct 05, 2026

Product Type

Hematological Reagents

Blood cell diluents

Invitro Diagnostics

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