AccessGUDID - DEVICE: ADVIA Centaur® Multi-Diluent 12 (00630414525549)

GUDID

Device Identifier (DI) Information

Brand Name: ADVIA Centaur® Multi-Diluent 12
Version or Model: 10335692
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 4786546
Company Name: Siemens Healthcare Diagnostics Inc.

Primary DI Number: 00630414525549
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 064608573 *Terms of Use

Device Description: Multidil 12 CSA - CENTAUR - CONS - 1x20mL

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?
58237	Buffered sample diluent IVD	A buffered diluent solution intended to be used as a consumable reagent during manual procedures or on-board an automated or semi-automated instrument (e.g., haematological cell analyser) for the processing, staining and/or testing of clinical laboratory specimens (e.g., whole blood).	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
MKW	CYCLOSPORINE

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K071455	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
Storage Environment Temperature: between 2 and 8 Degrees Celsius
Special Storage Condition, Specify: store upright

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: 091885ca-8853-45fb-9006-bee0b6f0ad9a
Public Version Date: June 13, 2023
Public Version Number: 6
DI Record Publish Date: September 24, 2016