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Qt-730

FDA UDI

Class II (US FDA UDI)

by Carestream Health, Inc.

Identity

Trade Name
QT-730 FDA UDI
Generic Name
Basic diagnostic x-ray system table, non-powered FDA UDI
Device Name
QT-730 RADIOGRAPHC ENCLOSED STYL TABLE FDA UDI
Model / Reference
QT-730 FDA UDI
Description
QT-730 RADIOGRAPHC ENCLOSED STYL TABLE FDA UDI

Identifiers

Catalog Number
6573521 FDA UDI
Primary DI / UDI-DI
60889976573525 FDA UDI
FDA Product Code
IZZ FDA UDI
GMDN Term
Basic diagnostic x-ray system table, non-powered FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1980 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: Basic diagnostic x-ray system table, non-powered

Qt-730 by Carestream Health, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Basic diagnostic x-ray system table, non-powered.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI cb9995b0-0b79-4817-8938-13a2cac4a3f4 34 fields · synced Jun 8, 2026