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DIAGCORE® Operational Module - Indonesia BPOM Medical Device Registration

DIAGCORE® Operational Module is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20102914566. The device is manufactured by LRE MEDICAL GMBH from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. INODIA.

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BPOM Registered
Risk Class Kelas Resiko : B
DIAGCORE® Operational Module
Analysis ID: AKL 20102914566

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

LRE MEDICAL GMBH

Country of Origin

Germany

Authorized Representative

PT. INODIA

AR Address

Perkantoran Kedoya Elok Plaza Blok DB no 24, Jalan Panjang, Kebon Jeruk

Registration Date

Jul 29, 2019

Expiry Date

Mar 06, 2024

Product Type

Clinical Laboratory Equipment

Instrumentation for clinical multiplex test systems.

Invitro Diagnostics

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