AccessGUDID - DEVICE: Urine Calibrator Set (04250317542397)

GUDID

Device Identifier (DI) Information

Brand Name: Urine Calibrator Set
Version or Model: 96033
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 96033
Company Name: Chromsystems Instruments + Chemicals GmbH

Primary DI Number: 04250317542397
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 328712260 *Terms of Use

Device Description: Urine Screening Standard Set MassTox® Drugs of Abuse Testing in urine

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?
55455	Multiple therapeutic drugs/drugs of abuse IVD, calibrator	A material which is used to establish known points of reference for an assay intended to be used for the qualitative and/or quantitative detection of multiple therapeutic drugs and drugs of abuse in a clinical specimen.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
DLJ	Calibrators, Drug Specific

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
Device Size Text, specify: 4x96003, 1x96003/0, 1x96024

Device Record Status

Public Device Record Key: 8f6c6148-45f4-4c0f-8f4b-be902c195de5
Public Version Date: January 02, 2020
Public Version Number: 1
DI Record Publish Date: December 25, 2019