Duns Number:315492330
Device Description: screwdriver blade cross slot 90mm hexagonal
Catalog Number
54.81.01
Brand Name
Medicon
Version/Model Number
54.81.01
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In GS1
MRI safety Status
MR Conditional
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
HRS
Product Code Name
Plate, fixation, bone
Public Device Record Key
0b62076f-bbe7-4019-b4cb-951badb2b7cb
Public Version Date
October 29, 2021
Public Version Number
1
DI Record Publish Date
October 21, 2021
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 | 7911 |
2 | A medical device with a moderate to high risk that requires special controls. | 1064 |