Duns Number:536935331
Device Description: The container is used in the transport and the sterilization of the QWIX® associated instr The container is used in the transport and the sterilization of the QWIX® associated instruments. It includes one combined base with reference 119941ND and one lid with reference 996200ND.The transport and sterilization containers are not intended to maintain sterility.
Catalog Number
-
Brand Name
QWIX®
Version/Model Number
119940ND
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"
Yes
For Single-Use
-
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
FSM
Product Code Name
TRAY, SURGICAL, INSTRUMENT
Public Device Record Key
867164ea-512b-40eb-9345-fd632a0e3a73
Public Version Date
July 08, 2021
Public Version Number
5
DI Record Publish Date
May 26, 2017
Package DI Number
None
Quantity per Package
-
Contains DI Package
-
Package Discontinue Date
-
Package Status
-
Package Type
-
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 388 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 235 |