Duns Number:783328149
Device Description: GRACEY CURETTE #3/4 HOLLOW
Catalog Number
-
Brand Name
J & J INSTRUMENTS
Version/Model Number
71-634
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)
-
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
EMS
Product Code Name
Curette, Periodontic
Public Device Record Key
82bf677e-ab74-4fbf-8f18-33937f3168f0
Public Version Date
November 18, 2019
Public Version Number
1
DI Record Publish Date
November 08, 2019
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 | 840 |
2 | A medical device with a moderate to high risk that requires special controls. | 6 |