Duns Number:092364462
Catalog Number
-
Brand Name
AccuTray™
Version/Model Number
5200103
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
December 09, 2019
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"
Yes
For Single-Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
-
Kit
-
Combination Product
Yes
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
OFT
Product Code Name
Spinal epidural anesthesia kit
Public Device Record Key
a1133810-304f-4612-bc71-cc10a0ab0045
Public Version Date
December 12, 2019
Public Version Number
4
DI Record Publish Date
August 26, 2016
Package DI Number
20809160001650
Quantity per Package
24
Contains DI Package
10809160001653
Package Discontinue Date
December 09, 2019
Package Status
Not in Commercial Distribution
Package Type
-
Device Class | Device Class Description | No of Devices |
---|---|---|
1 | A medical device with low to moderate risk that requires general controls | 548 |
2 | A medical device with a moderate to high risk that requires special controls. | 2798 |
U | Unclassified | 1 |