Duns Number:964569052
Device Description: HI-TORQUE TurnTrac Flex Guide Wire .014" Uncoated Straight Tip 300 cm
Catalog Number
1020012
Brand Name
HI-TORQUE TURNTRAC
Version/Model Number
1020012
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
DQX
Product Code Name
Wire, guide, catheter
Public Device Record Key
c85f5a68-63fc-4dd9-abf1-1437a2643392
Public Version Date
August 01, 2018
Public Version Number
2
DI Record Publish Date
May 26, 2018
Package DI Number
28717648222683
Quantity per Package
5
Contains DI Package
08717648222689
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
Case
| 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. | 964 |
| 3 | A medical device with high risk that requires premarket approval | 775 |