AccessGUDID - DEVICE: CLINITEK® Microalbumin 2 Reagent Strips (00630414548951)

GUDID

Device Identifier (DI) Information

Brand Name: CLINITEK® Microalbumin 2 Reagent Strips
Version or Model: 10317439
Commercial Distribution Status: In Commercial Distribution
Catalog Number: A2083C24
Company Name: Siemens Healthcare Diagnostics Inc.

Primary DI Number: 00630414548951
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 25
Labeler D-U-N-S® Number*: 064608573 *Terms of Use

Device Description: CLINITEK® Microalbumin 2 Reagent Strips are firm plastic strips that contain two reagent pads that test for albumin and creatinine in urine.

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?
54514	Multiple urine analyte IVD, kit, rapid colorimetric, clinical	A collection of reagents and other associated materials intended to be used for the qualitative and/or (semi-)quantitative detection of urine for multiple analytes within a short period relative to standard laboratory testing procedures, using a rapid colorimetric method. This is a rapid test commonly used in the laboratory or in point-of-care analyses to screen for non-microbial markers associated with a urinary tract infection (UTI) [e.g., leukocytes, blood, nitrites, proteins]. It is not intended to be used for self-testing.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
JFY	ENZYMATIC METHOD, CREATININE
CJG	TETRABROMO-M-CRESOLSULFONPHTHALEIN, ALBUMIN

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K972706	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: Do not store in direct sunlight.
Storage Environment Temperature: between 15 and 30 Degrees Celsius

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: e895ddf4-4dc4-4d0d-9323-b69950169e96
Public Version Date: November 28, 2022
Public Version Number: 7
DI Record Publish Date: September 24, 2016