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ACCUTREND Plus - Indonesia BPOM Medical Device Registration

ACCUTREND Plus is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101704835. The device is manufactured by LRE MEDICAL GMBH. from Germany, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. ROCHE INDONESIA.

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 : C
ACCUTREND Plus
Analysis ID: AKL 20101704835

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

LRE MEDICAL GMBH.

Country of Origin

Germany

Authorized Representative

PT. ROCHE INDONESIA

AR Address

Gedung AIA Central Lantai 36 Jl. Jend. Sudirman KAV. 48A RT/RW 003/004 Kelurahan Karet Semanggi

Registration Date

Jan 02, 2025

Expiry Date

Sep 04, 2029

Product Type

Clinical Chemistry Test System

Multi parameter clinical chemistry test system

Invitro Diagnostics

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