CDSCO UID IMP/MD/2022/000675_785d740094cf93a3c449ce1f2f046ada_7469beda26a81f07f7cc39044d978449

Direct Digitizer Computed Radiography

KONICA MINOLTA HEALTHCARE INDIA PRIVATE LIMITED·Device Class Class B·India CDSCO·Brand: DR System
Registration details
UID
IMP/MD/2022/000675_785d740094cf93a3c449ce1f2f046ada_7469beda26a81f07f7cc39044d978449
Device class
Class B
Brand name
DR System
Approving authority
CDSCO
Product information
The REGIUS SIGMA 2 is intended to read latent X-Ray image on the FP-1S housed in the RC -300, to output the image data and to erase the latent X-ray Image on the FP-1S
Similar products (3)
Other products with the same name or brand
Diagnostic Ultrasound
Brand: DR System
KONICA MINOLTA HEALTHCARE INDIA PRIVATE LIMITED
Class B
Diagnostic Ultrasound
Brand: DR System
KONICA MINOLTA HEALTHCARE INDIA PRIVATE LIMITED
Class B
Direct Digitizer
Brand: DR System
KONICA MINOLTA HEALTHCARE INDIA PRIVATE LIMITED
Class B
Other products from KONICA MINOLTA HEALTHCARE INDIA PRIVATE LIMITED
Products from the same license holder (10 products)
Diagnostic Ultrasound
Brand: ECO2/Aeroscan B1 pro
Class B
Diagnostic Ultrasound
Brand: ECO2/Aeroscan B1 pro
Class B
Color Doppler Ultrasound System
Brand: Sonoscape/Aeroscan
Class B
Diagnostic Ultrasound
Brand: Acclarix AX3/ Aeroscan CD10 Pro
Class B
Diagnostic Ultrasound
Brand: Acclarix AX3/ Aeroscan CD10 Pro
Class B
Diagnostic Ultrasound System
Brand: Aeroscan B2 pro
Class B
Diagnostic Ultrasound System
Brand: Aeroscan B2 pro
Class B
Diagnostic Ultrasound System
Brand: Aeroscan B2 pro
Class B
High Pressure Injector Syringe
Brand: MRI
Class B
High Pressure Injector Syringe
Brand: MRI
Class B
About this record

Direct Digitizer Computed Radiography is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2022/000675_785d740094cf93a3c449ce1f2f046ada_7469beda26a81f07f7cc39044d978449. This device is marketed under the brand name DR System. The license holder is KONICA MINOLTA HEALTHCARE INDIA PRIVATE LIMITED, and it is classified as Device Class Class B. The approving authority is CDSCO.

This page provides comprehensive regulatory information including complete registration details, license holder information, device classification, and related products. Pure Global AI offers free access to 71,807+ India medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.