Duns Number:964569052
Device Description: Hi-Torque Proceed 170T Angled Guide Wire w/Hydrophilic Coating .014” 300 cm
Catalog Number
1030902
Brand Name
Hi-Torque Proceed™
Version/Model Number
1030902
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
3499b018-ef6c-4b5b-a4d1-43a63c5b9561
Public Version Date
December 22, 2021
Public Version Number
2
DI Record Publish Date
October 18, 2020
Package DI Number
28717648321423
Quantity per Package
5
Contains DI Package
08717648321429
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 |