Duns Number:002348191
Device Description: DISP MANUAL RESUS,NEONATE W/FLOW DIVERTE
Catalog Number
5361
Brand Name
HUDSON RCI
Version/Model Number
IPN044933
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
K964719,K964719
Product Code
BTM
Product Code Name
Ventilator, emergency, manual (resuscitator)
Public Device Record Key
fbe57323-edfc-4e67-845c-7d7ae5bcce2a
Public Version Date
January 25, 2021
Public Version Number
5
DI Record Publish Date
October 16, 2015
Package DI Number
24026704551099
Quantity per Package
6
Contains DI Package
04026704551095
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
Box
| 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 |