Duns Number:002348191
Device Description: HUMID-VENT®, Compact, Straight w/ SOFTFLEX
Catalog Number
19402-BKH
Brand Name
Hudson RCI
Version/Model Number
IPN043769
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)
-
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
K964382,K964382
Product Code
CAH
Product Code Name
Filter, bacterial, breathing-circuit
Public Device Record Key
c95eab60-fc77-486e-9b77-100ac9efeba8
Public Version Date
December 22, 2021
Public Version Number
2
DI Record Publish Date
July 09, 2018
Package DI Number
24026704644869
Quantity per Package
25
Contains DI Package
14026704644862
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 |