AccessGUDID - DEVICE: Atellica IM CKMB (00630414598581)

GUDID

Device Identifier (DI) Information

Brand Name: Atellica IM CKMB
Version or Model: 10995531
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 10995531
Company Name: Siemens Healthcare Diagnostics Inc.

Primary DI Number: 00630414598581
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 5
Labeler D-U-N-S® Number*: 064608573 *Terms of Use

Device Description: CKMB Atellica IM - RGT 500T

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?
61000	Creatine kinase myocardial isoenzyme (CKMB) IVD, kit, chemiluminescent immunoassay	A collection of reagents and other associated materials intended to be used for the qualitative and/or quantitative detection of creatine kinase myocardial isoenzyme (CKMB) in a clinical specimen, using a chemiluminescent immunoassay method.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
JHS	DIFFERENTIAL RATE KINETIC METHOD, CPK OR ISOENZYMES

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K962126	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, Protect from light

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: cb37241c-51f1-46fd-9615-f707317bbc3b
Public Version Date: November 18, 2021
Public Version Number: 5
DI Record Publish Date: December 27, 2017