AccessGUDID - DEVICE: Atellica IM CA 19-9 MCM (00630414598192)

GUDID

Device Identifier (DI) Information

Brand Name: Atellica IM CA 19-9 MCM
Version or Model: 10995492
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 10995492
Company Name: Siemens Healthcare Diagnostics Inc.

Primary DI Number: 00630414598192
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 064608573 *Terms of Use

Device Description: CA 19-9 Atellica IM - Master Curve Material Kit 8 x 1 x 1.0mL

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?
38224	Cancer antigen 19-9 (CA19-9) 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 gastrointestinal and pancreatic cancer antigen 19-9 (CA19-9) 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 [?]
K031393	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, 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: 0a0494b7-d0a1-43d7-9560-8f56d0b2dcd3
Public Version Date: June 19, 2024
Public Version Number: 6
DI Record Publish Date: December 27, 2017