FDA UDI In Commercial Distribution 🇺🇸 United States

VITEK® DENSICHEK® Display Base

DI: 03573026605667 · Model: 422220 · BIOMERIEUX , INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
VITEK® DENSICHEK® Display Base
Primary DI
03573026605667
Version / Model
422220
Company Name
BIOMERIEUX , INC.
Labeler DUNS
086785110
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-12-06
Public Version
4
Public Version Date
2022-04-26
Public Version Status
Update
Public Device Record Key
fd12a274-2050-46c6-aef6-b2b97d79fda0

Device Description

The DISPLAY is part of the VITEK DensiCHEK that allows to read the McFarland value for a bacterial suspension. It is used for the Vitek instrument to prepare ID and AST test.

Device Characteristics

Single Use
No
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
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
No
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
36910 Photometer, absorbance/transmission, automated

Identifiers

Type ID
Primary 03573026605667

Premarket Submissions

Submission Number Supplement Number
K192110 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
-15 – 50 Degrees Celsius