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Vita XE CR System

FDA UDI

Class II (US FDA UDI)

by Carestream Health, Inc.

Identity

Trade Name
Vita XE CR System FDA UDI
Generic Name
Computed radiography digital imaging scanner FDA UDI
Device Name
NB VITA XE CR SOLUTION W / COMPUTER FDA UDI
Model / Reference
Vita XE CR System FDA UDI
Description
NB VITA XE CR SOLUTION W / COMPUTER FDA UDI

Identifiers

Catalog Number
1067685 FDA UDI
Primary DI / UDI-DI
60889971067685 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

No

FDA UDI

Category: Computed radiography digital imaging scanner

Vita XE CR System by Carestream Health, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Computed radiography digital imaging scanner.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Carestream Health, Inc.

Sources (1)

  • FDA UDI 812e897a-1d7a-4593-b03f-a1a1d63c79da 34 fields · synced Jun 8, 2026