FUJI MEDICAL DRY IMAGER - India CDSCO Medical Device Registration

FUJI MEDICAL DRY IMAGER is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2023/000776_4fde16924b74dfce8e35cb99c9543f85_7ec56139555615e7df54a2ee04aae915. This device is marketed under the brand name FCR PRIMA T2. The license holder is FUJIFILM INDIA Pvt. LTD.,, and it is classified as Device Class Class B. The approving authority is CDSCO.

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CDSCO Registered

Class Class B

FUJI MEDICAL DRY IMAGER

UID: IMP/MD/2023/000776_4fde16924b74dfce8e35cb99c9543f85_7ec56139555615e7df54a2ee04aae915

Brand Name

FCR PRIMA T2

License Holder

FUJIFILM INDIA Pvt. LTD.,

Device Class

Class B

Approving Authority

CDSCO

Product Information

Fuji Medical Dry Laser Imager DRYPIX EDGE (FCR PRIMA T2) is intended for providing the diagnostic Imaging data on the film by printing medical images transferred via DICOM network and archived in the PACS.This device is intended to be used by Healthcare professional

Class B

Brand: FDR SE Lite G43

Class B