Duns Number:053529939
Device Description: Cavity Cleanser 135ml Bottle
Catalog Number
B-2806A
Brand Name
Cavity Cleanser
Version/Model Number
B-2806A
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
K915668,K915668
Product Code
EBF
Product Code Name
MATERIAL, TOOTH SHADE, RESIN
Public Device Record Key
ae7b755c-7e42-4ee2-b6d7-e06a908b439c
Public Version Date
October 18, 2022
Public Version Number
1
DI Record Publish Date
October 10, 2022
Package DI Number
10810111542538
Quantity per Package
1
Contains DI Package
00810111542531
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
Item No: B-2816A
Device Class | Device Class Description | No of Devices |
---|---|---|
1 | A medical device with low to moderate risk that requires general controls | 335 |
2 | A medical device with a moderate to high risk that requires special controls. | 675 |