Duns Number:215591523
Catalog Number
-
Brand Name
Portex
Version/Model Number
C37091326-NLJ
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
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
BTC
Product Code Name
BAG, RESERVOIR
Public Device Record Key
0b90e9c6-e4c9-4862-85d7-7115c67bf812
Public Version Date
October 24, 2022
Public Version Number
4
DI Record Publish Date
October 05, 2016
Package DI Number
35019315059630
Quantity per Package
20
Contains DI Package
05019315059639
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
CARTON
Device Class | Device Class Description | No of Devices |
---|---|---|
1 | A medical device with low to moderate risk that requires general controls | 332 |
2 | A medical device with a moderate to high risk that requires special controls. | 431 |