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IMMULITE 2000 IGFBP-3 - Indonesia BPOM Medical Device Registration

IMMULITE 2000 IGFBP-3 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101323283. The device is manufactured by SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS LTD. from United Kingdom, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is SIEMENS HEALTHINEERS 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 : B
IMMULITE 2000 IGFBP-3
Analysis ID: AKL 20101323283

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

United Kingdom

Authorized Representative

SIEMENS HEALTHINEERS INDONESIA

AR Address

Perkantoran Hijau Arkadia Tower F, Lantai 18, Jl.Tahi Bonar Simatupang Kav. 88

Registration Date

Feb 05, 2025

Expiry Date

Feb 24, 2029

Product Type

Clinical Chemistry Test System

Immunoreactive insulin test system (kit & cair)

Invitro Diagnostics

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