Profile: Konica Minolta Medical Imaging USA Inc manufactures digital and traditional imaging products for diagnostic use by hospitals, imaging centers, clinics and private practice physicians. Our product DryPro family of laser imagers being used in health care places and hospitals.

The company was founded in 1963, has revenues of > USD 1 Billion, has ~31800 employees and is ISO 9001 certified.

FDA Registration Number: 2241281

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• (Dry & Wet) Laser Imagers

• Automatic Daylight X-Ray Film Handling Unit

• Automatic Radiographic Film Processor (FDA Code: IXW / 892.1900) An automatic radiographic film processor is a device intended to be used to develop, fix, wash, and dry automatically and continuously film exposed for medical purposes.

• Bench Mounted Hopper for X-Ray Film

• Blue Rare Earth X-Ray Film

• Computed Radiography

• Computed Radiography Accessories

• Computed Radiography Consulting Service

• Computed Radiography Kits

• Computed Radiography Service

• Consulting Services

• Contract Manufacturers

• CR (computed Radiography) Repair Services

• Densitometers (FDA Code: DXM / 870.1450) A densitometer is a device used to measure the transmission of light through an indicator in a sample of blood.

• Dental X-Ray Film

• Digital Radiographic Unit

• Film

• Film & Image Processors

• Film Image Accessories

• Film Processor Chemical

• Film Processors

• Film Processors Installation Service

• Film Processors Repair Services

• Green Sensitive Rare Earth X-Ray Film

• Laser (Dry & Wet) Imagers

• Laser Imager Accessories

• Laser Imagers Consulting Service

• Laser Imagers Installation Service

• Picture Archiving & Communications Systems

• Radiographic Film (FDA Code: IWZ / 892.1840) Radiographic film is a device that consists of a thin sheet of radiotransparent material coated on one or both sides with a photographic emulsion intended to record images during diagnostic radiologic procedures.

• Radiographic Film Cassette (FDA Code: IXA / 892.1850) A radiographic film cassette is a device intended for use during diagnostic x-ray procedures to hold a radiographic film in close contact with an x-ray intensifying screen and to provide a light-proof enclosure for direct exposure of radiographic film.

• Radiographic Intensifying Screen (FDA Code: EAM / 892.1960) A radiographic intensifying screen is a device that is a thin radiolucent sheet coated with a luminescent material that transforms incident x-ray photons into visible light and intended for medical purposes to expose radiographic film.

• Radiographic Sensitometer

• Radiographic X-Ray Film

• Radiology Workstations

• X-Ray Film

• X-Ray Film Block Shelter

• X-Ray Film Cabinet

• X-Ray Film Cassette Repairs

• X-ray Film Digitizers

• X-Ray Film Duplicators

• X-Ray Film Envelopes

• X-Ray Film Flexible Blockers

• X-Ray Film Holder

• X-Ray Film Keeping Self

• X-Ray Film Loading & Unloading Table

• X-Ray Film Marking Pencils

• X-Ray Film Processors

• X-Ray Film Scanners

• X-Ray Film Scanning Software