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Vue RIS

FDA UDI

Class I (US FDA UDI)

by Carestream Health, Inc.

Identity

Trade Name
Vue RIS FDA UDI
Generic Name
Radiology information system application software FDA UDI
Device Name
RIS SOFTWARE < 25K EXAMS / YEAR FDA UDI
Model / Reference
Vue RIS FDA UDI
Description
RIS SOFTWARE < 25K EXAMS / YEAR FDA UDI

Identifiers

Catalog Number
8671364 FDA UDI
Primary DI / UDI-DI
60889978671366 FDA UDI
FDA Product Code
LMD FDA UDI
GMDN Term
Radiology information system application software FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
892.2020 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

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Radiology information system application software

Vue RIS by Carestream Health, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Radiology information system application software.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 0f23a175-992c-47c1-976d-2df975a2be8c 35 fields · synced Jun 8, 2026