Duns Number:038305402
Device Description: 1/2 LITER HYPER SYSTEM W/MANOMETER,MASK & PRESS TUBE
Catalog Number
-
Brand Name
Ventlab
Version/Model Number
HS4251-X
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
-
Product Code
NHK
Product Code Name
Resuscitator,Manual,Non Self-Inflating
Public Device Record Key
5d3af7e3-a92f-4b1b-8c7b-063e16a8b51e
Public Version Date
March 29, 2018
Public Version Number
2
DI Record Publish Date
December 22, 2016
Package DI Number
20889483096656
Quantity per Package
10
Contains DI Package
10889483096659
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 | 82 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 612 |