Duns Number:061081477
Device Description: S/P POUCH SELF SEAL 3.5 X 9*200 #SCSS
Catalog Number
40750
Brand Name
SmartPractice
Version/Model Number
40750
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"
-
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
KCT
Product Code Name
Sterilization wrap containers, trays, cassettes & other accessories
Public Device Record Key
a391d57e-cd8f-48a9-9f78-4a478d18fdee
Public Version Date
November 08, 2019
Public Version Number
3
DI Record Publish Date
September 08, 2016
Package DI Number
D766407503
Quantity per Package
20
Contains DI Package
D766407501
Package Discontinue Date
-
Package Status
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 | 2 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 8 |
| U | Unclassified | 18 |