Duns Number:002348191
Device Description: ET TUBE, EXCHANGER, TTX, 4.0 - 6.0 MM
Catalog Number
5-24002
Brand Name
HUDSON RCI
Version/Model Number
IPN049129
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
K862347,K862347,K862347,K862347
Product Code
BTR
Product Code Name
Tube, tracheal (w/wo connector)
Public Device Record Key
bea6988c-d656-40c5-b6be-10d8cae82f5e
Public Version Date
January 20, 2021
Public Version Number
3
DI Record Publish Date
June 11, 2020
Package DI Number
44026704617928
Quantity per Package
10
Contains DI Package
34026704617921
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 | 3195 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 13747 |
| 3 | A medical device with high risk that requires premarket approval | 3 |
| U | Unclassified | 26 |