Duns Number:093608594
Catalog Number
1021529
Brand Name
WhisperPak, M572 V7 T956 C142 C955, 10
Version/Model Number
00
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"
-
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
BYE
Product Code Name
Attachment, breathing, positive end expiratory pressure
Public Device Record Key
420b101b-3b20-4542-a606-ddc99dc5c51f
Public Version Date
June 24, 2021
Public Version Number
5
DI Record Publish Date
September 05, 2017
Package DI Number
30884838082534
Quantity per Package
10
Contains DI Package
00884838082533
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
Multipack
Device Class | Device Class Description | No of Devices |
---|---|---|
1 | A medical device with low to moderate risk that requires general controls | 66 |
2 | A medical device with a moderate to high risk that requires special controls. | 61 |