Duns Number:007941230
Device Description: Tourniquet Perforated Roll Textured Blue Single-patient Use Polyisoprene Not Made With Nat Tourniquet Perforated Roll Textured Blue Single-patient Use Polyisoprene Not Made With Natural Rubber Latex 1inchx18inches MediChoice
Catalog Number
-
Brand Name
MediChoice
Version/Model Number
TRN1191
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)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
GAX
Product Code Name
TOURNIQUET, NONPNEUMATIC
Public Device Record Key
37c41fad-24f2-4a9d-9259-aa2b86db484f
Public Version Date
June 10, 2022
Public Version Number
3
DI Record Publish Date
August 31, 2020
Package DI Number
50885632128507
Quantity per Package
40
Contains DI Package
30885632128503
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 | 428 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 8754 |
| U | Unclassified | 1 |