Duns Number:174262477
Device Description: Debridement Kit
Catalog Number
-
Brand Name
Stradis Medical, LLC.
Version/Model Number
SR-255A
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In HIBCC
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
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
LRO
Product Code Name
General Surgery Tray
Public Device Record Key
6faf6f2a-0a91-4dd4-9f15-3241a4caa483
Public Version Date
June 17, 2022
Public Version Number
3
DI Record Publish Date
June 11, 2018
Package DI Number
M752SR255A5
Quantity per Package
20
Contains DI Package
M752SR255A0
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
outer box
Device Class | Device Class Description | No of Devices |
---|---|---|
1 | A medical device with low to moderate risk that requires general controls | 1226 |
2 | A medical device with a moderate to high risk that requires special controls. | 1431 |
U | Unclassified | 10 |