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FONMED HA 3 DIFF Diluent - Indonesia BPOM Medical Device Registration

FONMED HA 3 DIFF Diluent is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20208320668. The device is manufactured by EDAN INSTRUMENTS, INC. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. FOSUN DIAGNOSTICS INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : B
FONMED HA 3 DIFF Diluent
Analysis ID: AKL 20208320668

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. FOSUN DIAGNOSTICS INDONESIA

AR Address

FOSUN DIAGNOSTIK INDONESIA

Registration Date

Aug 07, 2023

Expiry Date

Aug 06, 2026

Product Type

Hematological Reagents

Blood cell diluents

Invitro Diagnostics

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