Duns Number:196548481
Device Description: 1.2mm Cross-Cut Fissure Carbide Bur
Catalog Number
2296-100-212
Brand Name
NA
Version/Model Number
2296100212
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
May 11, 2022
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
Yes
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
-
Product Code
EJL
Product Code Name
BUR, DENTAL
Public Device Record Key
30f3c5ef-263b-4439-b526-85cc19a16a68
Public Version Date
September 09, 2022
Public Version Number
4
DI Record Publish Date
September 23, 2018
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 | 2188 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 3183 |
| U | Unclassified | 60 |