FDA UDI In Commercial Distribution 🇺🇸 United States

VITEK®MS

DI: 03573026610418 · Model: VITEKMS SW v1.0 / FlexPrep v1.0 · BIOMERIEUX SA
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
VITEK®MS
Primary DI
03573026610418
Version / Model
VITEKMS SW v1.0 / FlexPrep v1.0
Company Name
BIOMERIEUX SA
Labeler DUNS
276816717
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-04-30
Public Version
1
Public Version Date
2019-05-08
Public Version Status
New
Public Device Record Key
00366b1d-8c49-4660-bc06-e8023cc2a8a6

Device Description

DVD to install VITEK MS SW v1.0 and VITEK MS FlexPrep v1.0 for clinical customers

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
No
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
PEX System, mass spectrometry, maldi tof, microorganism identification, cultured isolates

GMDN Terms

Code Name
61643 Microbial identification mass spectrometry system IVD

Identifiers

Type ID
Primary 03573026610418

Premarket Submissions

Submission Number Supplement Number
K162950 000
K181412 000