Duns Number:101571834
Device Description: Halo Vent Single IFAK. This device is a non-resorbable and non-sterile, occlusive wound dr Halo Vent Single IFAK. This device is a non-resorbable and non-sterile, occlusive wound dressing, intended to cover a wound and to provide a mechanical barrier. The vented seal allows air, gases, and fluids to escape from inside the chest through the device. Each package contains quantity: 1 Halo Vent.
Catalog Number
1216-10008
Brand Name
Halo
Version/Model Number
1216-10008
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)
Yes
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
NAD
Product Code Name
Dressing, Wound, Occlusive
Public Device Record Key
c136e4f9-f0a9-491a-be14-d5d45e775f5a
Public Version Date
March 10, 2021
Public Version Number
1
DI Record Publish Date
March 02, 2021
Package DI Number
00850010608112
Quantity per Package
200
Contains DI Package
00850010608105
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
-
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 8 |