FDA UDI In Commercial Distribution 🇺🇸 United States

VITEK®MS

DI: 03573026621698 · Model: VITEK MS SW V1.1 · BIOMERIEUX SA
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
VITEK®MS
Primary DI
03573026621698
Version / Model
VITEK MS SW V1.1
Company Name
BIOMERIEUX SA
Labeler DUNS
276816717
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-11-03
Public Version
1
Public Version Date
2021-11-11
Public Version Status
New
Public Device Record Key
4ee43db8-89b8-4241-b67c-e39f0606c470

Device Description

VITEK MS SW V1.1 + KB 3.2

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
QBN Mass spectrometry, MALDI TOF, microorganism identification, cultured isolates

GMDN Terms

Code Name
61643 Microbial identification mass spectrometry system IVD

Identifiers

Type ID
Primary 03573026621698

Premarket Submissions

Submission Number Supplement Number
K162950 000
K181412 000