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FCR ClearView CS Plus

FDA UDI

Class II (US FDA UDI)

by FUJIFILM Corporation

Identity

Trade Name
FCR ClearView CS Plus FDA UDI
Generic Name
Computed radiography digital imaging scanner FDA UDI
Device Name
The FUJI Computed Radiography System FCR ClearView CS Plus/CSm Plus performs Digital Radiography by using an Imaging Plate (IP) as the X-ray detection device. FDA UDI
Model / Reference
CR-IR 363 FDA UDI
Description
The FUJI Computed Radiography System FCR ClearView CS Plus/CSm Plus performs Digital Radiography by using an Imaging Plate (IP) as the X-ray detection device. FDA UDI

Identifiers

Primary DI / UDI-DI
04547410220575 FDA UDI
510(k) Number
K042023 FDA UDI
FDA Product Code
MQB FDA UDI
GMDN Term
Computed radiography digital imaging scanner FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1680 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Computed radiography digital imaging scanner

FCR ClearView CS Plus by FUJIFILM Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Computed radiography digital imaging scanner.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 4377551f-af4c-4e76-a024-ddfbb72519da 36 fields · synced May 30, 2026