FDA UDI In Commercial Distribution 🇺🇸 United States

Lambda light chains

DI: 08058056681263 · Model: A26849 · SENTINEL CH. SPA
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Lambda light chains
Primary DI
08058056681263
Version / Model
A26849
Catalog Number
A26849
Company Name
SENTINEL CH. SPA
Labeler DUNS
429572365
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-07-29
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
526f85a0-e79a-415a-9e23-2fed082d55ee

Device Description

The Lambda light chains assay is an in vitro diagnostic test used for the quantitative determination of Immunoglobulin bound and free lambda light chains (LAMBDA) in serum and Li-heparin plasma by immunoturbidimetry. It is intended to measure Immunoglobulin Lambda light chains (bound and free) using Synchron LX20 and Unicel DxC 600 Systems.

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
DEH Lambda, Antigen, Antiserum, Control

GMDN Terms

Code Name
53801 Kappa/lambda light chain immunoglobulin IVD, reagent

Identifiers

Type ID
Primary 08058056681263

Customer Contacts

Phone
9999999999

Premarket Submissions

Submission Number Supplement Number
K083601 000

Device Sizes

Type Value Unit Text
Total Volume 120 Milliliter

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Store between 2 and 8 degrees Celsius