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Qg-Tv-F

FDA UDI

Class I (US FDA UDI)

by Carestream Health, Inc.

Identity

Trade Name
QG-TV-F FDA UDI
Generic Name
X-ray system computer, diagnostic, general-purpose FDA UDI
Device Name
QG-TV10-F TECHVISION QS-550 WITH Q-VISIO FDA UDI
Model / Reference
QG-TV-F FDA UDI
Description
QG-TV10-F TECHVISION QS-550 WITH Q-VISIO FDA UDI

Identifiers

Catalog Number
6573299 FDA UDI
Primary DI / UDI-DI
60889976573297 FDA UDI
FDA Product Code
IZO FDA UDI
GMDN Term
X-ray system computer, diagnostic, general-purpose FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
892.1700 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: X-ray system computer, diagnostic, general-purpose

Qg-Tv-F by Carestream Health, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as X-ray system computer, diagnostic, general-purpose.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 205d6d3b-2537-42fa-8c06-3fc853a8c0f3 34 fields · synced Jun 8, 2026