Duns Number:080448429
Device Description: Base Assembly Aluminum (L)25 (W)12 (H)4
Catalog Number
122 BASE.ASSY.AL.25.12.4
Brand Name
EZ-TRAX™
Version/Model Number
122 BASE.ASSY.AL.25.12.4
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
FSM
Product Code Name
Tray, Surgical, Instrument
Public Device Record Key
cb05a407-4bbb-453c-8d86-5d6e8a541530
Public Version Date
September 16, 2022
Public Version Number
3
DI Record Publish Date
February 14, 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 | 57 |
2 | A medical device with a moderate to high risk that requires special controls. | 91 |