AccessGUDID - DEVICE: CMP 200 DR (00885310000144)

GUDID

Device Identifier (DI) Information

Brand Name: CMP 200 DR
Version or Model: VZW2556RH2
Commercial Distribution Status: In Commercial Distribution
Catalog Number:
Company Name: Communications & Power Industries Canada Inc

Primary DI Number: 00885310000144
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 202887311 *Terms of Use

Device Description: Generator, High-Voltage, X-Ray, Diagnostic, CMP200, RAD, 32kW, 400V

Device Characteristics

What MRI safety information does the labeling contain?	Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437):	No
Device labeled as "Not made with natural rubber latex":	No
For Single-Use:	No
Prescription Use (Rx):	No
Over the Counter (OTC):	No
Kit:	No
Combination Product:	No
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P):	No

GMDN

[?]

GMDN Term Code	GMDN Term Name	GMDN Term Definition	GMDN Term Status [?]	Implantable?
37604	Diagnostic x-ray system generator, stationary	A generator which is an integral component of a stationary diagnostic x-ray system, e.g., a system intended to be operated at a fixed location within a facility or mobile imaging van. It is used to regulate incoming voltage and current to provide an x-ray tube with the power needed to produce an x-ray beam of the desired voltage (kV) and current (mA). It typically comprises a control assembly (console) and high voltage transformer assembly, or it is of a mono-tank generator design and includes transformer, constant potential, inverter and capacitor discharge generator designs.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
IZO	Generator, High-Voltage, X-Ray, Diagnostic

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
Premarket Submission Number Not Available/Not Released

Device Exempt from Premarket Submission: Yes CLOSE

Sterilization

Device Packaged as Sterile: No
Requires Sterilization Prior to Use: No

Sterilization Method [?]
No Sterilization Methods Found

Storage and Handling

[?]

Storage and Handling
Storage Environment Temperature: between -25 and 70 Degrees Celsius
Storage Environment Humidity: between 5 and 95 Percent (%) Relative Humidity
Storage Environment Atmospheric Pressure: between 525 and 795 Millimeter of Mercury

Clinically Relevant Size

[?]

Size Type Text
Length: 25.7 Inch
Width: 13.7 Inch
Height: 24.3 Inch

Device Record Status

Public Device Record Key: 1511e9dc-d048-43f3-b45c-e759d7c12b86
Public Version Date: October 14, 2020
Public Version Number: 2
DI Record Publish Date: July 24, 2020