Duns Number:131480662
Device Description: The BLAST® Bandage was designed to provide the ability to quickly package traumatic amputa The BLAST® Bandage was designed to provide the ability to quickly package traumatic amputations, burns, and large pattern wounds with minimal use of supplies and minimal effort. The BLAST® Bandage provides a 20" X 20" treatment area, but packs to about the size of a 4” combat bandage.Our large non-adherent wound pad can be easily wrapped around limbs and secured with the attached elastic wrap. It provides a large sterile protective covering for shrapnel wounds or burns. With such a large coverage area, the Blast® Bandage is large enough to cover the entire back or chest of most casualties.The BLAST® Bandage also offers a removable occlusive layer that will cover a 19"x 19" area or can be used to cover abdominal contents minimizing the loss of heat and moisture.As with our other bandages, the "brakes" on the bandage help prevent accidental unrolling of the elastic wrap during high stress application. These brakes are especially helpful during the dressing of amputations. By providing multiple points of adhesion, the brakes prevent slippage of the elastic during the wrapping process. This creates a more secure, effective bandage and decreases the chance of the wound being exposed during movement.
Catalog Number
BLAST
Brand Name
Blast Bandage
Version/Model Number
A
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)
-
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
MHW
Product Code Name
Dressing, Compression
Public Device Record Key
21a3fc60-303f-4c78-abcb-2e8683cdb3bc
Public Version Date
February 21, 2022
Public Version Number
2
DI Record Publish Date
October 15, 2020
Package DI Number
None
Quantity per Package
-
Contains DI Package
-
Package Discontinue Date
-
Package Status
-
Package Type
-
Device Class | Device Class Description | No of Devices |
---|---|---|
1 | A medical device with low to moderate risk that requires general controls | 39 |
2 | A medical device with a moderate to high risk that requires special controls. | 1 |