AKIRON NEO - Indonesia BPOM Medical Device Registration
AKIRON NEO is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20304420083. The device is manufactured by MEDIPAN GMBH from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. 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 : 2
Manufacturer
MEDIPAN GMBHCountry of Origin
Germany
Authorized Representative
PT. SEGMED DISTRIBUTION INDONESIAAR Address
SEGMED DISTRIBUSI INDONESIA
Registration Date
Sep 12, 2024
Expiry Date
Apr 21, 2027
Product Type
Immunology Laboratory Equipment and Reagents
Immunofluorometer equipment
Invitro Diagnostics
Fluorobeads™ T Lymphocyte
ONE LAMBDA INC.
ONE LAMBDA PE-Conjugated Goat Anti-Human IgG
ONE LAMBDA INC.
Fluorobeads™ B Lymphocyte
ONE LAMBDA INC.
FlowPRA™ Negative Control
ONE LAMBDA INC
FlowPRA ™ Class I Positive Control
ONE LAMBDA INC.
LABScan 3D Verification Kit
LUMINEX CORPORATION
LABScreen ™ Negative Control
ONE LAMBDA INC.
LABScan 3D Calibration Kit
LUMINEX CORPORATION
Lyophilized Class I Complement
ONE LAMBDA INC.
Lyophilized Class II Complement
ONE LAMBDA INC.