Mobile Dr

FDA UDI

Class I (US FDA UDI)

by Communications & Power Industries Canada Inc

Identity

Trade Name: MOBILE DR FDA UDI
Generic Name: Diagnostic x-ray system generator, mobile FDA UDI
Device Name: Generator, High-Voltage, X-Ray, Diagnostic, MOBILE DR, RAD, 32kW, 240V FDA UDI
Model / Reference: VZW2559RH1 FDA UDI
Description: Generator, High-Voltage, X-Ray, Diagnostic, MOBILE DR, RAD, 32kW, 240V FDA UDI

Identifiers

Primary DI / UDI-DI: 00885310000342 FDA UDI
FDA Product Code: IZO FDA UDI
GMDN Term: Diagnostic x-ray system generator, mobile 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Dimensions & Sizes

Size: Length — 14.7 Inch FDA UDI
Width — 14.6 Inch FDA UDI
Height — 13.6 Inch FDA UDI

Category: Diagnostic x-ray system generator, mobile

Mobile Dr by Communications & Power Industries Canada Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Communications & Power Industries Canada Inc

Sources (1)

FDA UDI cbba24f2-8fab-4879-8e53-6eb451140cdf 35 fields · synced May 30, 2026