Duns Number:806806220
Catalog Number
-
Brand Name
Sheathes
Version/Model Number
5-40040
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
Yes
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
OIP
Product Code Name
Radiology-Diagnostic Kit
Public Device Record Key
966d2b86-b8f0-4d80-a5b7-4a5c79238e00
Public Version Date
June 10, 2022
Public Version Number
3
DI Record Publish Date
July 31, 2018
Package DI Number
20842418103126
Quantity per Package
3
Contains DI Package
10842418103129
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
CASE
Device Class | Device Class Description | No of Devices |
---|---|---|
2 | A medical device with a moderate to high risk that requires special controls. | 1 |