Duns Number:002348191
Device Description: ET TUBE, SHER-I-BRONCH, LS, 35 FR
Catalog Number
5-16035
Brand Name
HUDSON RCI
Version/Model Number
IPN048995
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In GS1
MRI safety Status
MR Unsafe
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
K180253,K180253,K180253,K180253
Product Code
CBI
Product Code Name
TUBE, TRACHEAL/BRONCHIAL, DIFFERENTIAL VENTILATION (W/WO CONNECTOR)
Public Device Record Key
4a990d49-84b0-4128-b44a-e3a87db84883
Public Version Date
July 01, 2021
Public Version Number
7
DI Record Publish Date
September 20, 2018
Package DI Number
44026704617393
Quantity per Package
4
Contains DI Package
34026704617396
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 |