DEMEDITEC Measles IgG ELISA - Indonesia BPOM Medical Device Registration
DEMEDITEC Measles IgG ELISA is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303025936. The device is manufactured by DEMEDITEC DIAGNOSTICS GMBH. from Germany, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. FRIMUST ADIJAYA UTAMA.
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
DEMEDITEC DIAGNOSTICS GMBH.Country of Origin
Germany
Authorized Representative
PT. FRIMUST ADIJAYA UTAMAAR Address
JL. PEMUDA NO. M3
Registration Date
May 07, 2024
Expiry Date
Jan 29, 2029
Product Type
Serological Reagents
Rubeola (measles) virus serological reagents.
Invitro Diagnostics
MONOBIND CA 15-3 AccuBind ELISA Test System
MONOBIND, INC
QSURE Multi-Ligand Quality Control
MONOBIND, INC
QSURE Anti-H.Pylori Quality Control
MONOBIND, INC
DEMEDITEC ANA Hep Screen ELISA
DEMEDITEC DIAGNOSTICS GMBH
SCHEBO Master Quick-Prep™
SCHEBO BIOTECH
SCHEBO M2-PK™ ELISA Stool Test
SCHEBO BIOTECH
Rubella IgM ACCUBIND ELISA Test System
MONOBIND, INC
AFP-CEA-PSA Cancer Panel AccuBind VAST ELISA Test System
MONOBIND, INC
MONOBIND Toxoplasma IgM AccuBind ELISA Test System
MONOBIND, INC
MONOBIND Total T3-Total T4-TSH AccuBind VAST ELISA Test System
MONOBIND, INC