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Varex Imaging

FDA UDI

Class I (US FDA UDI)

by Varex Imaging Corporation

Identity

Trade Name
Varex Imaging FDA UDI
Generic Name
Ionization chamber radiation measuring probe FDA UDI
Device Name
An Ionization Chamber is a device that is placed between the patient and an x-ray image receptor to assist the Automatic Exposure Control (AEC) in delivering the proper x-ray dose in medical radiography. This is a device out of the Ionization Chambers series. FDA UDI
Model / Reference
ICX1217B FDA UDI
Description
An Ionization Chamber is a device that is placed between the patient and an x-ray image receptor to assist the Automatic Exposure Control (AEC) in delivering the proper x-ray dose in medical radiography. This is a device out of the Ionization Chambers series. FDA UDI

Identifiers

Primary DI / UDI-DI
08718755003000 FDA UDI
FDA Product Code
IZO FDA UDI
GMDN Term
Ionization chamber radiation measuring probe FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
892.1700 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Ionization chamber radiation measuring probe

Varex Imaging by Varex Imaging Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ionization chamber radiation measuring probe.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 2a7b736e-01d9-4f6e-878f-61b47f4fc09d 33 fields · synced Jun 9, 2026