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Green Tem 512

FDA UDI

Class I (US FDA UDI)

by Flow X-Ray Corp.

Identity

Trade Name
GREEN TEM 512 FDA UDI
Generic Name
Dental x-ray film, non-screen FDA UDI
Device Name
GREEN SENSITIVE PANO FILM, 5X12" 50 PER BOX FDA UDI
Model / Reference
18095-G FDA UDI
Description
GREEN SENSITIVE PANO FILM, 5X12" 50 PER BOX FDA UDI

Identifiers

Primary DI / UDI-DI
H66518095G1 FDA UDI
FDA Product Code
IWZ FDA UDI
GMDN Term
Dental x-ray film, non-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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Dental x-ray film, non-screen

Green Tem 512 by Flow X-Ray Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental x-ray film, non-screen.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Flow X-Ray Corp.

Sources (1)

  • FDA UDI 08d1c8ae-1702-4dea-aa5b-148b3c13599b 34 fields · synced Jun 1, 2026