AccessGUDID - DEVICE: N FLC SUPPLEMENTARY REAGENT (00630414237473)

GUDID

Device Identifier (DI) Information

Brand Name: N FLC SUPPLEMENTARY REAGENT
Version or Model: 10873660
Commercial Distribution Status: In Commercial Distribution
Catalog Number: OPJC05
Company Name: Siemens Healthcare Diagnostics Products GmbH

Primary DI Number: 00630414237473
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 388240673 *Terms of Use

Device Description: Immunonephelometric determination of free light chains (FLC) type kappa and type lambda 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?
53801	Kappa/lambda light chain immunoglobulin IVD, reagent	A substance or reactant intended to be used together with a parent IVD to perform a specific function in an assay that is used for the quantitative measurement of kappa and/or lambda light chain immunoglobulins in a clinical specimen.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
DFH	KAPPA, ANTIGEN, ANTISERUM, CONTROL
DEH	LAMBDA, ANTIGEN, ANTISERUM, CONTROL

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K171742	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: 729b6166-9d6d-46a8-b9a2-79d3f315b8c3
Public Version Date: November 18, 2021
Public Version Number: 4
DI Record Publish Date: October 08, 2018