Duns Number:106712748
Catalog Number
-
Brand Name
Portex
Version/Model Number
100/126/030
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
K790312,K790312,K790312
Product Code
BTR
Product Code Name
Tube, tracheal (w/wo connector)
Public Device Record Key
195eca69-cd82-460d-b7bc-31d993545ffe
Public Version Date
December 01, 2020
Public Version Number
5
DI Record Publish Date
September 01, 2015
Package DI Number
55019315056763
Quantity per Package
10
Contains DI Package
35019315056769
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
Pallet
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 3 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 686 |
| 3 | A medical device with high risk that requires premarket approval | 2 |
| U | Unclassified | 1 |