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.
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.
Risk Classification
Product Class
Kelas : 2
Manufacturer
LRE MEDICAL GMBHCountry of Origin
Germany
Authorized Representative
PT. INODIAAR 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.
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