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T-Mat E

FDA UDI

Class I (US FDA UDI)

by Carestream Health, Inc.

Identity

Trade Name
T-MAT E FDA UDI
Generic Name
Dental x-ray film, screen FDA UDI
Device Name
T-MAT E 100SH 15x30cm film FDA UDI
Model / Reference
T-MAT E FDA UDI
Description
T-MAT E 100SH 15x30cm film FDA UDI

Identifiers

Catalog Number
5216742 FDA UDI
Primary DI / UDI-DI
40889975216740 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

No

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Dental x-ray film, screen

T-Mat E by Carestream Health, Inc. — Class I — 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 a87e3926-d6e8-465c-892d-a54698e47d91 35 fields · synced Jun 8, 2026