AccessGUDID - DEVICE: Urine Calibrator Set (04250317537706)

GUDID

Device Identifier (DI) Information

Brand Name: Urine Calibrator Set
Version or Model: 80839
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 80839
Company Name: Chromsystems Instruments + Chemicals GmbH

Primary DI Number: 04250317537706
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 328712260 *Terms of Use

Device Description: 6PLUS1® Multilevel Urine Calibrator Set MassChrom® VMA, HVA, 5-HIAA

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?
60610	HVA/VMA/5HIAA IVD, calibrator	A material which is used to establish known points of reference for an assay intended to be used for the quantitative measurement of homovanillic acid (HVA), vanillylmandelic acid (VMA) and 5-hydroxyindoleacetic acid (5HIAA) in a clinical specimen.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
JIX	Calibrator, Multi-Analyte Mixture

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: less than -18 Degrees Celsius

Clinically Relevant Size

[?]

Size Type Text
Total Volume: 1 Milliliter
Device Size Text, specify: 7 Vials

Device Record Status

Public Device Record Key: 63ad2db1-5a87-47f4-9778-937b4d1eed77
Public Version Date: April 01, 2019
Public Version Number: 1
DI Record Publish Date: March 22, 2019