AccessGUDID - DEVICE: RadQual (00850020470464)

GUDID

Device Identifier (DI) Information

Brand Name: RadQual
Version or Model: BM08-57
Commercial Distribution Status: In Commercial Distribution
Catalog Number:
Company Name: RADQUAL, LLC

Primary DI Number: 00850020470464
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 008841076 *Terms of Use

Device Description: Co 57 Rod Source

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?
38318	Radionuclide source, quality assurance	A naturally occurring, accelerator produced, or reactor produced radioactive isotope used as a source of radiation in a variety of quality assurance (QA) tests, e.g., markers, daily constancy test, accuracy tests, linearity test, radiation detector operation and calibration of analytical and radiation field instruments. A QA radionuclide source comes in a variety of physical forms, e.g., sealed source, plated/foil source, embedded source or contained radioactive liquids or gels. It may be selected for a particular QA use because of the radiation it emits (alpha particles, beta particles, neutrons, gamma rays, x-rays), its energy spectrum or physical half-life.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
IXD	Source, Calibration, Sealed, Nuclear

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: dc17c041-c0a7-47a4-a783-2d7dd25a2461
Public Version Date: August 11, 2020
Public Version Number: 1
DI Record Publish Date: August 03, 2020

Alternative and Additional Identifiers Additional Identifiers

Package DI

[?]

Package DI Number	Quantity per Package	Contains DI Package	Package Discontinue Date	Package Status	Package Type
No Package DIs found

Secondary DI

[?]

Issuing Agency [?]	Secondary DI Number
No Secondary DIs found

Unit of Use DI

[?]

Unit of Use DI Number: No Unit of Use DI Numbers Found CLOSE

Direct Marking (DM)

[?]

Device Subject to Direct Marking (DM), but Excepted: No
DM DI Different from Primary DI: No
DM DI Number: None
CLOSE

Production Identifier(s) in UDI

[?]

Lot or Batch Number: No
Serial Number: No
Expiration Date: No
Manufacturing Date: No
Donation Identification Number: No CLOSE

Customer Contact

[?]

No Customer Contact currently defined

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