Duns Number:122561087
Device Description: BD BBL™ Sensi-Disc™ Ceftaroline - 30 µg
Catalog Number
232231
Brand Name
BD BBL™ Sensi-Disc™ Ceftaroline - 30 µg
Version/Model Number
232231
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In GS1
MRI safety Status
Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)
-
Device labeled as "Not made with natural rubber latex"
-
For Single-Use
-
Prescription Use (Rx)
Yes
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
K112586,K112586
Product Code
JTN
Product Code Name
SUSCEPTIBILITY TEST DISCS, ANTIMICROBIAL
Public Device Record Key
e569d554-5f08-4ef3-9f05-176b7b4be348
Public Version Date
July 06, 2018
Public Version Number
3
DI Record Publish Date
May 19, 2016
Package DI Number
None
Quantity per Package
-
Contains DI Package
-
Package Discontinue Date
-
Package Status
-
Package Type
-
Device Class | Device Class Description | No of Devices |
---|---|---|
1 | A medical device with low to moderate risk that requires general controls | 611 |
2 | A medical device with a moderate to high risk that requires special controls. | 614 |
3 | A medical device with high risk that requires premarket approval | 36 |
U | Unclassified | 4 |