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D-Speed

FDA UDI

Class II (US FDA UDI)

by Carestream Health, Inc.

Identity

Trade Name
D-Speed FDA UDI
Generic Name
Dental x-ray film, non-screen FDA UDI
Device Name
100PKT FLASH D-SPEED PERFECT FLM SIZE2 FDA UDI
Model / Reference
D-Speed FDA UDI
Description
100PKT FLASH D-SPEED PERFECT FLM SIZE2 FDA UDI

Identifiers

Catalog Number
8626483 FDA UDI
Primary DI / UDI-DI
40889978626485 FDA UDI
FDA Product Code
NOF FDA UDI
GMDN Term
Dental x-ray film, non-screen FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3661 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

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: Dental x-ray film, non-screen

D-Speed 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, non-screen.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 556be414-a3db-4455-aff5-fa04a4c24053 35 fields · synced Jun 8, 2026