Cmp 200 Dr

FDA UDI

Class I (US FDA UDI)

by Communications & Power Industries Canada Inc

Identity

Trade Name: CMP 200 DR FDA UDI
Generic Name: Diagnostic x-ray system generator, stationary FDA UDI
Device Name: Generator, High-Voltage, X-Ray, Diagnostic ,CMP200, RAD, 32kW, 208/230V,3PH. FDA UDI
Model / Reference: VZW2556RH4 FDA UDI
Description: Generator, High-Voltage, X-Ray, Diagnostic ,CMP200, RAD, 32kW, 208/230V,3PH. FDA UDI

Identifiers

Primary DI / UDI-DI: 00885310000168 FDA UDI
FDA Product Code: IZO FDA UDI
GMDN Term: Diagnostic x-ray system generator, stationary 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 — 25.7 Inch FDA UDI
Width — 13.7 Inch FDA UDI
Height — 24.3 Inch FDA UDI

Category: Diagnostic x-ray system generator, stationary

Cmp 200 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 91c38621-2c7a-498c-9ad2-bd189ed6ba9a 35 fields · synced May 30, 2026