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Vision Xr

FDA UDI

Class I (US FDA UDI)

by Benco Dental Supply Co.

Identity

Trade Name
VISION XR FDA UDI
Generic Name
Dental x-ray film, screen FDA UDI
Device Name
Vision XR Panoramic Film 6"x12" Box of 100 FDA UDI
Model / Reference
4232-279 FDA UDI
Description
Vision XR Panoramic Film 6"x12" Box of 100 FDA UDI

Identifiers

Primary DI / UDI-DI
00366975024886 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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Dental x-ray film, screen

Vision Xr by Benco Dental Supply Co. — 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 1cff4ecb-0ffa-419b-a0a9-e8a3d4cb8f02 34 fields · synced Jun 8, 2026