AccessGUDID - DEVICE: N LP(a) Standard SY (00630414285009)

GUDID

Device Identifier (DI) Information

Brand Name: N LP(a) Standard SY
Version or Model: 10873686
Commercial Distribution Status: In Commercial Distribution
Catalog Number: OQCV07
Company Name: Siemens Healthcare Diagnostics Products GmbH

Primary DI Number: 00630414285009
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 3
Labeler D-U-N-S® Number*: 388240673 *Terms of Use

Device Description: Calibration of Lp(a) assay on BN Systems

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?
41417	Lipoprotein A IVD, calibrator	A material which is used to establish known points of reference for an assay intended to be used for the quantitative measurement of lipoprotein A lipid in a clinical specimen.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
JIS	Calibrator, primary

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K013126	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: 401ecc3f-fcc9-4ec2-932a-2e4f8a36ef17
Public Version Date: November 18, 2021
Public Version Number: 2
DI Record Publish Date: October 12, 2020