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LABTEST AST-GOT Liquiform - Indonesia BPOM Medical Device Registration

LABTEST AST-GOT Liquiform is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101813361. The device is manufactured by LABTEST DIAGNOSTICA S.A. from Brazil, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. WHIRA PITOE USAHABERSAMA.

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
LABTEST AST-GOT Liquiform
Analysis ID: AKL 20101813361

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Brazil

Authorized Representative

PT. WHIRA PITOE USAHABERSAMA

AR Address

RUKO BUARAN PERSADA NO. 10, JL. JEND.POL.SOEKAMTO RT.008/06,KEL.DUREN SAWIT

Registration Date

Oct 19, 2020

Expiry Date

Jan 08, 2025

Product Type

Clinical Chemistry Test System

Aspartate amino transferase (AST/SGOT) test system (kit & cair)

Invitro Diagnostics

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