FDA UDI In Commercial Distribution 🇺🇸 United States

VITEK® MS-FA

DI: 03573026555559 · Model: VITEK® MS-FA · BIOMERIEUX SA
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
VITEK® MS-FA
Primary DI
03573026555559
Version / Model
VITEK® MS-FA
Company Name
BIOMERIEUX SA
Labeler DUNS
276816717
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-12-19
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
2a41b005-cca0-4c83-81c4-da2b443a60ec

Device Description

VITEK ® MS - FA is used to pretreat yeasts to facilitate their identification according to the MALDI - TOF method. It is used exclusively with the VITEK ® MS instrument.

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
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
PEX System, Mass Spectrometry, Maldi Tof, Microorganism Identification, Cultured Isolates

GMDN Terms

Code Name
61643 Microbial identification mass spectrometry system IVD

Identifiers

Type ID
Package 03573026362843
Primary 03573026555559

Premarket Submissions

Submission Number Supplement Number
DEN130013 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
2 – 8 Degrees Celsius