Duns Number:107105876
Device Description: MODIFIED INSTRUMENT ENDPLATE ELEVATOR, ANGLED 24 degree
Catalog Number
698343746
Brand Name
NA
Version/Model Number
698343746
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
-
Product Code
HTE
Product Code Name
ELEVATOR
Public Device Record Key
d8ade1c1-d845-425a-8650-f5b1fc9dd9c2
Public Version Date
June 10, 2022
Public Version Number
2
DI Record Publish Date
March 06, 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 | 5839 |
2 | A medical device with a moderate to high risk that requires special controls. | 2784 |
U | Unclassified | 20 |