AccessGUDID - DEVICE: Atellica IM Syph QC (00630414599892)

GUDID

Device Identifier (DI) Information

Brand Name: Atellica IM Syph QC
Version or Model: 10995676
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 10995676
Company Name: Siemens Healthcare Diagnostics Inc.

Primary DI Number: 00630414599892
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 064608573 *Terms of Use

Device Description: Syphillis (Syph) QC Kit Atellica IM - CLT 2 x 2 x 7.0mL

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?
37733	Treponema pallidum total antibody IVD, control	A material which is used to verify the performance of an assay intended to be used for the qualitative and/or quantitative detection of total antibodies to Treponema pallidum bacteria in a clinical specimen.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
LIP	ENZYME LINKED IMMUNOABSORPTION ASSAY, TREPONEMA PALLIDUM

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K112343	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, Protect from Light, Do not freeze, Resuspend.
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: 775e8d3d-50c5-4968-ba6b-6eb60b365abe
Public Version Date: November 18, 2021
Public Version Number: 2
DI Record Publish Date: September 24, 2020