T-Mat L/Ra

FDA UDI

Class I (US FDA UDI)

by Carestream Health, Inc.

Identity

Trade Name: T-MAT L/RA FDA UDI
Generic Name: Dental x-ray film, screen FDA UDI
Device Name: T-MAT L/RA 50SH 8x10in film FDA UDI
Model / Reference: T-MAT L/RA FDA UDI
Description: T-MAT L/RA 50SH 8x10in film FDA UDI

Identifiers

Catalog Number: 1589852 FDA UDI
Primary DI / UDI-DI: 40889971589855 FDA UDI
FDA Product Code: IWZ FDA UDI
GMDN Term: Dental x-ray film, screen FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 892.1840 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Dental x-ray film, screen

T-Mat L/Ra by Carestream Health, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Carestream Health, Inc.

Sources (1)

FDA UDI 06e993c3-2552-4eb4-9f16-74a76d57c779 35 fields · synced Jun 8, 2026