InviMag® Universal Kit / KF96 - Indonesia BPOM Medical Device Registration
InviMag® Universal Kit / KF96 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10204220293. The device is manufactured by INVITEK MOLECULAR GMBH from Germany, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is SEGMED DISTRIBUTION 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.
Risk Classification
Product Class
Kelas : 1
Manufacturer
INVITEK MOLECULAR GMBHCountry of Origin
Germany
Authorized Representative
SEGMED DISTRIBUTION INDONESIAAR Address
SEGMED DISTRIBUSI INDONESIA
Registration Date
Oct 20, 2022
Expiry Date
May 01, 2024
Product Type
Reagents and Specimen Providers
General purpose reagent.
Invitro Diagnostics
FREND TSH Neo
NANOENTEK INC
LABType PE Conjugated Streptavidin
ONE LAMBDA INC.
BIOREX AHG Coomb's
BIOREX DIAGNOSTICS LTD.
BIOREX Serological Albumin 22 %
BIOREX DIAGNOSTICS LTD.
AKLIDES ANA Plus
MEDIPAN GMBH
RespiFinder 2SMART
PATHOFINDER B.V.
BIOREX Pregnancy Latex Tests
BIOREX DIAGNOSTICS LTD.
ANA 18 Line
GA GENERIC ASSAYS GMBH
BIOREX RF Latex Test
BIOREX DIAGNOSTICS LTD.
BIOREX Anti-A Monoclonal
BIOREX DIAGNOSTICS LTD.

