| Primary Device ID | 28717648015759 |
| NIH Device Record Key | bef1299d-edcf-43ac-bad6-9236765ae513 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | HI-TORQUE IRON MAN |
| Version Model Number | 1001311J |
| Catalog Number | 1001311J |
| 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 |
| Phone | +1(800)227-9902 |
| AV.CUSTOMERCARE@AV.ABBOTT.COM |
| Special Storage Condition, Specify | Between 0 and 0 *Stored in a dry, dark, cool place |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 08717648015755 [Primary] |
| GS1 | 28717648015759 [Package] Contains: 08717648015755 Package: Case [5 Units] In Commercial Distribution |
| DQX | WIRE, GUIDE, CATHETER |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 6 |
| Public Version Date | 2020-03-23 |
| Device Publish Date | 2016-06-30 |
| 28717648015759 | HI-TORQUE IRON MAN Guide Wire .014 J Tip 3.0 cm x 300 cm |
| 28717648015742 | HI-TORQUE IRON MAN Guide Wire .014 J Tip 3.0 cm x 190 cm |
| 08717648013652 | HI-TORQUE IRON MAN Guide Wire .014 Straight Tip 3.0 cm x 300 cm |
| 28717648013649 | HI-TORQUE IRON MAN Guide Wire .014 Straight Tip 3.0 cm x 190 cm |