← Back to catalogue

Mobile Nano

FDA UDI

Class I (US FDA UDI)

by Communications & Power Industries Canada Inc

Identity

Trade Name
MOBILE NANO FDA UDI
Generic Name
Diagnostic x-ray system generator, mobile FDA UDI
Device Name
Generator, High-Voltage, X-Ray, Diagnostic, MOBILE NANO, RAD, 8kW, 62-76V FDA UDI
Model / Reference
VZW2566RTDM FDA UDI
Description
Generator, High-Voltage, X-Ray, Diagnostic, MOBILE NANO, RAD, 8kW, 62-76V FDA UDI

Identifiers

Primary DI / UDI-DI
00885310000427 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

No

FDA UDI

Single Use

No

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 457.0 Millimeter FDA UDI
Height — 353.6 Millimeter FDA UDI

Category: Diagnostic x-ray system generator, mobile

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

Similar devices

Also classified as Diagnostic x-ray system generator, mobile.

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

Sources (1)

  • FDA UDI a6b25679-7e19-456f-9a5e-940080f343c6 35 fields · synced May 30, 2026