BODITECH RF IgM Control - Indonesia BPOM Medical Device Registration
BODITECH RF IgM Control is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20305520065. The device is manufactured by BODITECH MED INC., from Korea, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. BODITECH MED 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
BODITECH MED INC.,Country of Origin
Korea
Authorized Representative
PT. BODITECH MED INDONESIAAR Address
Ruko Alam Sutera, Jalur Sutera Kavling 25 B-C No.1
Registration Date
Feb 05, 2025
Expiry Date
Feb 05, 2029
Product Type
Immunological Test System
Rheumatoid factor immunological test system.
Invitro Diagnostics
AFIAS D-Dimer Neo
AFIAS PSA
AFIAS CRP
AFIAS Cyfra 21-1
AFIAS NT-proBNP
AFIAS TSH
AFIAS PCT X
BODITECH TSH Plus Control
AFIAS Vitamin D Neo
BODITECH Calprotectin Control
AFIAS NT-proBNP
BODITECH MED INC.,
AFIAS Tn-I Plus
BODITECH WITH INC.
AFIAS Ferritin
BODITECH WITH INC.
AFIAS D-Dimer Neo
BODITECH MED INC.,
AFIAS PSA
BODITECH MED INC.,
AFIAS Cyfra 21-1
BODITECH MED INC.,
AFIAS CRP
BODITECH MED INC.,
AFIAS TSH
BODITECH MED INC.,
AFIAS PCT X
BODITECH MED INC.,
BODITECH TSH Plus Control
BODITECH MED INC.,