← Back to catalogue

Maxi-Dent D Speed Vinyl

FDA UDI

Class I (US FDA UDI)

by Flow X-Ray Corp.

Identity

Trade Name
Maxi-Dent D Speed Vinyl FDA UDI
Generic Name
Dental x-ray film, non-screen FDA UDI
Device Name
Minimax Maxi-Dent D Speed Vinyl pack, 100/bx, Dental X-Ray Film Size 2 FDA UDI
Model / Reference
28194 FDA UDI
Description
Minimax Maxi-Dent D Speed Vinyl pack, 100/bx, Dental X-Ray Film Size 2 FDA UDI

Identifiers

Primary DI / UDI-DI
00812045032119 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

Maxi-Dent D Speed Vinyl 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Flow X-Ray Corp.

Sources (1)

  • FDA UDI 241956da-a8e6-4b56-bdf0-1939061c511f 33 fields · synced May 29, 2026