HI-TORQUE INTERMEDIATE 22317H
GUDID 08717648079757
HI-TORQUE Intermediate Guide Wire w/Hydrocoat .014 Straight 3.0 cm x 190 cm
ABBOTT VASCULAR INC.
Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use| Primary Device ID | 08717648079757 |
| NIH Device Record Key | 38c809c8-fa26-4c59-a251-01ba8c63a8fb |
| Commercial Distribution Discontinuation | 2021-01-17 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | HI-TORQUE INTERMEDIATE |
| Version Model Number | 22317H |
| Catalog Number | 22317H |
| Company DUNS | 964569052 |
| Company Name | ABBOTT VASCULAR INC. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
Customer Support Contacts
Operating and Storage Conditions
| Special Storage Condition, Specify | Between 0 and 0 *Stored in a dry, dark, cool place |
| Special Storage Condition, Specify | Between 0 and 0 *Stored in a dry, dark, cool place |
| Special Storage Condition, Specify | Between 0 and 0 *Stored in a dry, dark, cool place |
| Special Storage Condition, Specify | Between 0 and 0 *Stored in a dry, dark, cool place |
| Special Storage Condition, Specify | Between 0 and 0 *Stored in a dry, dark, cool place |
| Special Storage Condition, Specify | Between 0 and 0 *Stored in a dry, dark, cool place |
| Special Storage Condition, Specify | Between 0 and 0 *Stored in a dry, dark, cool place |
| Special Storage Condition, Specify | Between 0 and 0 *Stored in a dry, dark, cool place |
| Special Storage Condition, Specify | Between 0 and 0 *Stored in a dry, dark, cool place |
| Special Storage Condition, Specify | Between 0 and 0 *Stored in a dry, dark, cool place |
| Special Storage Condition, Specify | Between 0 and 0 *Stored in a dry, dark, cool place |
| Special Storage Condition, Specify | Between 0 and 0 *Stored in a dry, dark, cool place |
| Special Storage Condition, Specify | Between 0 and 0 *Stored in a dry, dark, cool place |
| Special Storage Condition, Specify | Between 0 and 0 *Stored in a dry, dark, cool place |
| Special Storage Condition, Specify | Between 0 and 0 *Stored in a dry, dark, cool place |
| Special Storage Condition, Specify | Between 0 and 0 *Stored in a dry, dark, cool place |
| Special Storage Condition, Specify | Between 0 and 0 *Stored in a dry, dark, cool place |
| Special Storage Condition, Specify | Between 0 and 0 *Stored in a dry, dark, cool place |
| Special Storage Condition, Specify | Between 0 and 0 *Stored in a dry, dark, cool place |
| Special Storage Condition, Specify | Between 0 and 0 *Stored in a dry, dark, cool place |
| Special Storage Condition, Specify | Between 0 and 0 *Stored in a dry, dark, cool place |
| Special Storage Condition, Specify | Between 0 and 0 *Stored in a dry, dark, cool place |
| Special Storage Condition, Specify | Between 0 and 0 *Stored in a dry, dark, cool place |
| Special Storage Condition, Specify | Between 0 and 0 *Stored in a dry, dark, cool place |
| Special Storage Condition, Specify | Between 0 and 0 *Stored in a dry, dark, cool place |
| Special Storage Condition, Specify | Between 0 and 0 *Stored in a dry, dark, cool place |
| Special Storage Condition, Specify | Between 0 and 0 *Stored in a dry, dark, cool place |
| Special Storage Condition, Specify | Between 0 and 0 *Stored in a dry, dark, cool place |
| Special Storage Condition, Specify | Between 0 and 0 *Stored in a dry, dark, cool place |
| Special Storage Condition, Specify | Between 0 and 0 *Stored in a dry, dark, cool place |
| Special Storage Condition, Specify | Between 0 and 0 *Stored in a dry, dark, cool place |
| Special Storage Condition, Specify | Between 0 and 0 *Stored in a dry, dark, cool place |
| Special Storage Condition, Specify | Between 0 and 0 *Stored in a dry, dark, cool place |
| Special Storage Condition, Specify | Between 0 and 0 *Stored in a dry, dark, cool place |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 08717648079757 [Primary] |
| GS1 | 28717648079751 [Package] Package: Case [5 Units] Discontinued: 2021-01-17 Not in Commercial Distribution |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K974773
FDA Product Code
| DQX | WIRE, GUIDE, CATHETER |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2024-02-07 |
| Device Publish Date | 2016-02-12 |
On-Brand Devices [HI-TORQUE INTERMEDIATE]
| 28717648079881 | HI-TORQUE Intermediate Guide Wire .014 J Tip 3.0 cm x 190 cm |
| 08717648079832 | HI-TORQUE Intermediate Guide Wire .014 Straight Tip 3.0 cm x 190 cm |
| 28717648079805 | HI-TORQUE Intermediate Guide Wire w/Hydrocoat .014 J Tip 3.0 cm x 190 cm |
| 08717648079771 | HI-TORQUE Intermediate Guide Wire w/Hydrocoat .014 Straight Tip 3.0 cm x 300 cm |
| 08717648079757 | HI-TORQUE Intermediate Guide Wire w/Hydrocoat .014 Straight 3.0 cm x 190 cm |
Trademark Results [HI-TORQUE INTERMEDIATE]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 HI-TORQUE INTERMEDIATE 73616437 1488271 Live/Registered |
ADVANCED CARDIOVASCULAR SYSTEMS, INC. 1986-08-25 |
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.