FDA UDI In Commercial Distribution 🇺🇸 United States

Bulk Analyzer Reagent Pack

DI: 00850031114005 · Model: 01-10019 · Selux Diagnostics, Inc.
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Bulk Analyzer Reagent Pack
Primary DI
00850031114005
Version / Model
01-10019
Company Name
Selux Diagnostics, Inc.
Labeler DUNS
079715313
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-12-20
Public Version
1
Public Version Date
2024-12-30
Public Version Status
New
Public Device Record Key
460e0ed1-51a4-4361-ba34-e905f4000f4b

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
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
LTW Susceptibility Test Cards, Antimicrobial
LTT Panels, Test, Susceptibility, Antimicrobial
LON System, Test, Automated, Antimicrobial Susceptibility, Short Incubation

GMDN Terms

Code Name
56737 Antimicrobial susceptibility analyser IVD

Identifiers

Type ID
Primary 00850031114005

Premarket Submissions

Submission Number Supplement Number
K211748 000
K211759 000