Duns Number:053187985
Device Description: Composite Placement, DE, Titanium-Nitride Coated, Paddle 55A/Acorn #22B
Catalog Number
-
Brand Name
NORDENT MANUFACTURING INC
Version/Model Number
REPFI55AT-22BT
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
EKD
Product Code Name
Instrument, Cutting, Operative
Public Device Record Key
9112d8a5-b02e-423c-9fe2-3e29e6377365
Public Version Date
January 08, 2021
Public Version Number
1
DI Record Publish Date
December 31, 2020
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 | 5029 |
2 | A medical device with a moderate to high risk that requires special controls. | 5 |