FDA UDI Not in Commercial Distribution 🇺🇸 United States

VITEK® 2 AST-ST01

DI: 03573026529741 · Model: VITEK®2 AST-ST01 · BIOMERIEUX , INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
VITEK® 2 AST-ST01
Primary DI
03573026529741
Version / Model
VITEK®2 AST-ST01
Company Name
BIOMERIEUX , INC.
Labeler DUNS
086785110
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-01-09
Public Version
4
Public Version Date
2021-11-18
Public Version Status
Update
Public Device Record Key
d68e1a47-9406-4ce3-9403-618d144b9f24
Distribution End Date
2019-10-08

Device Description

The VITEK ® 2 Streptococcus Susceptibility Card is intended for use with the VITEK 2 to determine the susceptibility of S. pneumo , beta-hemolytic Strep, & Viridans Strep

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
LON System, Test, Automated, Antimicrobial Susceptibility, Short Incubation

GMDN Terms

Code Name
58605 General-microorganism antimicrobial susceptibility culture medium IVD

Identifiers

Type ID
Package 03573026345334
Primary 03573026529741

Premarket Submissions

Submission Number Supplement Number
K111599 000
K111893 000
K111909 000
K111976 000
K112000 000
K112075 000
K112129 000
K112228 000
K113305 000
K121100 000
K121863 000
K122359 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
2 – 8 Degrees Celsius