AccessGUDID - DEVICE: Stratus® CS Acute Care™ MYO TestPak (00842768004605)

GUDID

Device Identifier (DI) Information

Brand Name: Stratus® CS Acute Care™ MYO TestPak
Version or Model: 10445079
Commercial Distribution Status: In Commercial Distribution
Catalog Number: CMYO
Company Name: Siemens Healthcare Diagnostics Inc.

Primary DI Number: 00842768004605
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 100
Labeler D-U-N-S® Number*: 005088112 *Terms of Use

Device Description: The Stratus® CS Acute Care(TM) Myoglobin (MYO) method is an in vitro diagnostic test for the quantitative measurement of myoglobin in heparinized plasma.

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:	Yes
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?
61390	Myoglobin IVD, kit, fluorescent immunoassay	A collection of reagents and other associated materials intended to be used for the quantitative measurement of myoglobin in a clinical specimen, using a fluorescent immunoassay method.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
DDR	MYOGLOBIN, ANTIGEN, ANTISERUM, CONTROL
JHX	FLUOROMETRIC METHOD, CPK OR ISOENZYMES
JIT	CALIBRATOR, SECONDARY
MMI	IMMUNOASSAY METHOD, TROPONIN SUBUNIT

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K051650	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

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: fd4e53b0-29c9-4f8c-b6c7-223464c76563
Public Version Date: November 19, 2021
Public Version Number: 5
DI Record Publish Date: September 24, 2016