Duns Number:042075700
Device Description: The CompressAR Large Round Disc is a sterile, single use product that is attached to the C The CompressAR Large Round Disc is a sterile, single use product that is attached to the CompressAR System Stand to apply compression to the femoral artery during hemostasis. The Model 5123 is a large, round flat disc (2" dia.).
Catalog Number
150-0123-06
Brand Name
CompressAR Large Round Disc
Version/Model Number
5123
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
K831337,K831337,K831337
Product Code
DQO
Product Code Name
Catheter, Intravascular, Diagnostic
Public Device Record Key
06ebd276-c5f5-45a2-ad87-ffed22c72a28
Public Version Date
July 06, 2018
Public Version Number
3
DI Record Publish Date
September 24, 2016
Package DI Number
20815614020184
Quantity per Package
12
Contains DI Package
10815614020187
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 | 3 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 27 |
| U | Unclassified | 1 |