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Select Cassette with LANEX Medium Screens

FDA UDI

Class II (US FDA UDI)

by Carestream Health, Inc.

Identity

Trade Name
Select Cassette with LANEX Medium Screens FDA UDI
Generic Name
Dental x-ray film, screen FDA UDI
Device Name
18X24CM KDK SLCT CASS W/LANX MED C1 FDA UDI
Model / Reference
Select Cassette with LANEX Medium Screens FDA UDI
Description
18X24CM KDK SLCT CASS W/LANX MED C1 FDA UDI

Identifiers

Catalog Number
1017664 FDA UDI
Primary DI / UDI-DI
60889971017666 FDA UDI
FDA Product Code
IXA FDA UDI
EAM FDA UDI
GMDN Term
Dental x-ray film, screen FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1850 FDA UDI
892.1960 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: X-ray film cassette, automatic film changingDental x-ray film, screen

Select Cassette with LANEX Medium Screens by Carestream Health, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental x-ray film, screen.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 2ab3b4cc-5636-4d9c-ab3d-60756bcbea4e 34 fields · synced Jun 8, 2026