Duns Number:009831413
Device Description: Quala Pouch 2 3/4 X 9 BULK
Catalog Number
LAD2790
Brand Name
Quala
Version/Model Number
LAD2790
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)
Yes
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
6d2550ad-32bd-4ad7-bde6-5aa278db5293
Public Version Date
November 08, 2019
Public Version Number
3
DI Record Publish Date
February 13, 2017
Package DI Number
D023LAD27903
Quantity per Package
5000
Contains DI Package
D023LAD27901
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
Case
Device Class | Device Class Description | No of Devices |
---|---|---|
1 | A medical device with low to moderate risk that requires general controls | 224 |
2 | A medical device with a moderate to high risk that requires special controls. | 192 |