FRESENIUS Conox 2D QM7000-M GB2 - Indonesia BPOM Medical Device Registration
FRESENIUS Conox 2D QM7000-M GB2 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20402320119. The device is manufactured by FRESENIUS VIAL S.A.S. from France, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. FRESENIUS KABI 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
FRESENIUS VIAL S.A.S.Country of Origin
France
Authorized Representative
PT. FRESENIUS KABI INDONESIAAR Address
Menara Bidakara 1 Lt.19, Jl. Gatot Subroto Kav 71 - 73 Menteng Dalam, Tebet, Jakarta Selatan 12870
Registration Date
Aug 17, 2023
Expiry Date
Nov 29, 2027
Product Type
Monitoring Anesthesia Equipment
Electrical peripheral nerve stimulator.
Non Radiation Electromedics
CONOX Pediatric Sensor
FRESENIUS KABI (NANCHANG) CO., LTD.
FRESENIUS KABI 3 Way Stopcock
FRESENIUS KABI (NANCHANG) CO., LTD.
FRESENIUS 3-Way-Stopcock
CLINICO MEDICAL SP. Z.O.O.
AMICUS Separator and Accessories
FRESENIUS KABI WARRENDALE.
VS 10 DEHP-Free
CLINICO MEDICAL SP. Z O.O.
AmiCORE Apheresis Kit - Single Needle with Two Platelet Containers and PAS Connector
FENWAL INTERNATIONAL, INC.
FRESENIUS Amicore Apheresis Kit - Single Needle
FENWAL INTERNATIONAL INC.
AGILIA SP PCA WIFI ID
FRESENIUS VIAL
AMICORE Apheresis Kit - Single Needle with Two Platelet Containers
FENWAL INTERNATIONAL INC.
COMPOLAB TM Cuvette
EKF-DIAGNOSTIC GMBH