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DSI HDL-c direct FS - Indonesia BPOM Medical Device Registration

DSI HDL-c direct FS is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101421925. The device is manufactured by DIASYS DIAGNOSTIC SYSTEM, GMBH from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. INDONESIAN SYSTEM DIAGNOSTICS.

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
DSI HDL-c direct FS
Analysis ID: AKL 20101421925

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Germany

Authorized Representative

PT. INDONESIAN SYSTEM DIAGNOSTICS

AR Address

Jl. Meruya Ilir Ruko Intercon Blok A-IX No 12B, Jakarta 11630

Registration Date

Oct 03, 2024

Expiry Date

Sep 30, 2027

Product Type

Clinical Chemistry Test System

Cholesterol (total) test system (kit & cair)

Invitro Diagnostics

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