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QUANTILAB LDH-P - Indonesia BPOM Medical Device Registration

QUANTILAB LDH-P is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101121925. The device is manufactured by INSTRUMENTATION LABORATORY SPA, from Italy, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. DEXA ARFINDO PRATAMA.

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
QUANTILAB LDH-P
Analysis ID: AKL 20101121925

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Italy

Authorized Representative

PT. DEXA ARFINDO PRATAMA

AR Address

Jl. Dr. Ir. H. Soekarno 407 RT 1 RW 9

Registration Date

Dec 16, 2024

Expiry Date

Sep 23, 2029

Product Type

Clinical Chemistry Test System

Lactate dehydrogenase isoenzymes test system (kit & cair)

Invitro Diagnostics

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