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PATHFAST™ - Indonesia BPOM Medical Device Registration

PATHFAST™ is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10102220110. The device is manufactured by LSI MEDIENCE CORPORATION. from Japan, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. NUSANTARA BINA DIAGNOSTIKA.

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 : A
PATHFAST™
Analysis ID: AKL 10102220110

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Japan

Authorized Representative

PT. NUSANTARA BINA DIAGNOSTIKA

AR Address

Pertokoan Bali View No. 35 Jl. Rajawali Pisangan Ciputat, Tangerang Selatan

Registration Date

Nov 07, 2022

Expiry Date

Oct 13, 2025

Product Type

Clinical Laboratory Equipment

Colorimeter, photometer, or spectrophotometer for clinical use.

Invitro Diagnostics

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