AccessGUDID - DEVICE: ADVIA Centaur® VALP MCM (00630414527369)

GUDID

Device Identifier (DI) Information

Brand Name: ADVIA Centaur® VALP MCM
Version or Model: 10322232
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number: 5261307
Company Name: Siemens Healthcare Diagnostics Inc.

Primary DI Number: 00630414527369
Issuing Agency: GS1
Commercial Distribution End Date: August 21, 2023
Device Count: 1
Labeler D-U-N-S® Number*: 064608573 *Terms of Use

Device Description: Valproic Acid Master Curve Material Set - CENTAUR - CONS

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?
55432	Valproic acid therapeutic drug monitoring IVD, control	A material which is used to verify the performance of an assay intended to be used for the quantitative measurement and therapeutic monitoring of the central nervous system drug valproic acid in a clinical specimen.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
JJX	Single (specified) analyte controls (assayed and unassayed)

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K013959	000

Device Exempt from Premarket Submission: No 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
Special Storage Condition, Specify: store upright
Storage Environment Temperature: between 2 and 8 Degrees Celsius

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: f18e4ae3-d5a2-40a5-aa2b-c3fc9aaeb082
Public Version Date: July 17, 2024
Public Version Number: 7
DI Record Publish Date: September 24, 2016