FDA UDI Not in Commercial Distribution 🇺🇸 United States

Etest® CEFOTAXIME

DI: 03573026548735 · Model: Etest® CEFOTAXIME · BIOMERIEUX SA
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Etest® CEFOTAXIME
Primary DI
03573026548735
Version / Model
Etest® CEFOTAXIME
Company Name
BIOMERIEUX SA
Labeler DUNS
276816717
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-11-18
Public Version
5
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
b19ce292-6096-40f3-894a-681b2ca23774
Distribution End Date
2016-11-18

Device Description

Etest is a quantitative technique for determining susceptibility of clinically significant bacteria. It provides a gradient of 15 doubling dilutions for MIC determination.

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
JWY Manual Antimicrobial Susceptibility Test Systems

GMDN Terms

Code Name
43144 Cefotaxime minimum inhibitory concentration (MIC) IVD

Identifiers

Type ID
Package 03573026252540
Primary 03573026548735

Premarket Submissions

Submission Number Supplement Number
K981137 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
-20 – 8 Degrees Celsius