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ERBA Lyse - Diff - Indonesia BPOM Medical Device Registration

ERBA Lyse - Diff is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20208320504. The device is manufactured by ERBA LACHEMA S.R.O from Czech Republic, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is ELBA LAB MEDIKA.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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BPOM Registered
Risk Class Kelas Resiko : B
ERBA Lyse - Diff
Analysis ID: AKL 20208320504

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

ERBA LACHEMA S.R.O

Country of Origin

Czech Republic

Authorized Representative

ELBA LAB MEDIKA

AR Address

GRAHA BUMI INDAH LANTAI II ROOM 2005, JL. RAYA KALIMALANG KAV. AGRARIA NO. 8-0 RT/RW 002/016 KEL. DUREN SAWIT KEC. DUREN SAWIT JAKARTA TIMUR

Registration Date

Mar 28, 2023

Expiry Date

Jun 23, 2027

Product Type

Hematological Reagents

Red cell lysing reagent.

Invitro Diagnostics

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