AccessGUDID - DEVICE: Dosimeter Dosimax plus A HV (EIBAVD02017900)

GUDID

Device Identifier (DI) Information

Brand Name: Dosimeter Dosimax plus A HV
Version or Model: VD0201790
Commercial Distribution Status: In Commercial Distribution
Catalog Number: VD0201790
Company Name: IBA Dosimetry GmbH

Primary DI Number: EIBAVD02017900
Issuing Agency: HIBCC
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 332599307 *Terms of Use

Device Description: Dosimeter with internal high voltage supply according to IEC 61674 for use with ionization chamber DCT10-RS. Designed for measurements at all types of X-ray units.

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):	Yes
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?
38385	Diagnostic x-ray system quality assurance device	An instrument intended to be used to assess the performance of diagnostic x-ray equipment for quality assurance (QA) purposes; it is typically intended to measure, display, and record one or more x-ray parameter(s) [e.g., kVp, mAs, dose, exposure time]. It may be placed in the field of view and/or be connected to the x-ray equipment, and may have various forms (e.g., handheld or desktop unit with sensor and dedicated software).	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
LHO	Instrument, Quality-Assurance, Radiologic

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
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: f8117d78-0916-4b9d-82cb-41069156ac9a
Public Version Date: July 04, 2022
Public Version Number: 2
DI Record Publish Date: October 26, 2020