FDA UDI In Commercial Distribution 🇺🇸 United States

VITEK® 2 AST-N802

DI: 03573026617844 · Model: VITEK® 2 AST-N802 · BIOMERIEUX , INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
VITEK® 2 AST-N802
Primary DI
03573026617844
Version / Model
VITEK® 2 AST-N802
Company Name
BIOMERIEUX , INC.
Labeler DUNS
086785110
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-05-19
Public Version
2
Public Version Date
2022-05-10
Public Version Status
Update
Public Device Record Key
ff061e68-d9c0-47fb-8b3d-f5614f5b0e18

Device Description

VITEK® 2 Gram Negative Susceptibility Card is intended for use with the VITEK 2 Systems to determine the susceptibility of clinically significant aerobic gram-negative bacilli

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 03573026617752
Primary 03573026617844

Premarket Submissions

Submission Number Supplement Number
K072038 000
K091899 000
K110106 000
K113200 000
K161217 000
K161227 000
K162737 000
K163563 000
K172731 000
K183415 000
N50510 082
N50510 097
N50510 107
N50510 118
N50510 124

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
2 – 8 Degrees Celsius