VCOMIN Fetal Doppler - Indonesia BPOM Medical Device Registration
VCOMIN Fetal Doppler is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21101515528. The device is manufactured by VCOMIN TECHNOLOGY LIMITED. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. GRAHA MEGATAMA 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
VCOMIN TECHNOLOGY LIMITED.Country of Origin
China
Authorized Representative
PT. GRAHA MEGATAMA INDONESIAAR Address
BIZ PARK 3 COMMERCIAL ESTATE BLOK E NOMOR 9, JALAN SULTAN AGUNG KM 28.5
Registration Date
Nov 12, 2024
Expiry Date
Jan 24, 2029
Product Type
Obstetric and Gynecological Monitoring Equipment
Fetal ultrasonic monitor and accessories.
Non Radiation Electromedics
VCOMIN NESCO Ezcheck Fetal Doppler
NESCO Ezcheck Fetal Doppler
VCOMIN Fetal Doppler
VCOMIN Fetal Doppler
VCOMIN Fetal Doppler
A CLASS Fetal Doppler
NESCO Ezcheck Fetal Doppler
A Class Fetal Doppler
VITRO Flow Chip Hybridization Reagents Type I (Auto)
VITRO S.A
VITRO hybriSpot24
VITRO S.A.
VITRO Sepsis Flow Chip Kit (Hybridiation Reagents)
VITRO S.A.
VITRO hybriSpot12
VITRO S.A.
VITRO Sepsis Flow Chip Kit (PCR Reagents)
VITRO S.A.
VITRO HybriSpot 12 PCR Auto
VITRO S.A.
VITRO Bacterial CNS Flow Chip Kit (Hybridization Reagents)
VITRO S.A.
VITRO Bacterial CNS Flow Chip Kit (PCR Reagents)
VITRO S.A.
VITRO HPV Direct Flow Chip Kit (Hybridization Reagents)
VITRO S.A
VITRO STD Direct Flow Chip Kit (PCR Reagents)
VITRO S.A.

