Duns Number:092364462
Catalog Number
-
Brand Name
ACCUTRAY
Version/Model Number
5200049
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
March 25, 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
41059160-ab4d-44bc-9e03-62aa6ae24537
Public Version Date
August 14, 2020
Public Version Number
5
DI Record Publish Date
August 26, 2016
Package DI Number
20809160001575
Quantity per Package
24
Contains DI Package
10809160001578
Package Discontinue Date
March 25, 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 |