| Primary Device ID | 28717648124079 |
| NIH Device Record Key | a86ec138-0e13-4fe4-9927-e6b4967c1500 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | LOC |
| Version Model Number | 1012068-10 |
| Catalog Number | 1012068-10 |
| 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 | |
| Phone | +1(800)227-9902 |
| AV.CUSTOMERCARE@AV.ABBOTT.COM | |
| Phone | +1(800)227-9902 |
| AV.CUSTOMERCARE@AV.ABBOTT.COM | |
| Phone | +1(800)227-9902 |
| AV.CUSTOMERCARE@AV.ABBOTT.COM | |
| Phone | +1(800)227-9902 |
| AV.CUSTOMERCARE@AV.ABBOTT.COM | |
| Phone | +1(800)227-9902 |
| AV.CUSTOMERCARE@AV.ABBOTT.COM | |
| Phone | +1(800)227-9902 |
| AV.CUSTOMERCARE@AV.ABBOTT.COM | |
| Phone | +1(800)227-9902 |
| AV.CUSTOMERCARE@AV.ABBOTT.COM | |
| Phone | +1(800)227-9902 |
| AV.CUSTOMERCARE@AV.ABBOTT.COM | |
| Phone | +1(800)227-9902 |
| AV.CUSTOMERCARE@AV.ABBOTT.COM | |
| Phone | +1(800)227-9902 |
| AV.CUSTOMERCARE@AV.ABBOTT.COM | |
| Phone | +1(800)227-9902 |
| AV.CUSTOMERCARE@AV.ABBOTT.COM |
| Special Storage Condition, Specify | Between 0 and 0 *Store in a dry, dark, cool place |
| Special Storage Condition, Specify | Between 0 and 0 *Store in a dry, dark, cool place |
| Special Storage Condition, Specify | Between 0 and 0 *Store in a dry, dark, cool place |
| Special Storage Condition, Specify | Between 0 and 0 *Store in a dry, dark, cool place |
| Special Storage Condition, Specify | Between 0 and 0 *Store in a dry, dark, cool place |
| Special Storage Condition, Specify | Between 0 and 0 *Store in a dry, dark, cool place |
| Special Storage Condition, Specify | Between 0 and 0 *Store in a dry, dark, cool place |
| Special Storage Condition, Specify | Between 0 and 0 *Store in a dry, dark, cool place |
| Special Storage Condition, Specify | Between 0 and 0 *Store in a dry, dark, cool place |
| Special Storage Condition, Specify | Between 0 and 0 *Store in a dry, dark, cool place |
| Special Storage Condition, Specify | Between 0 and 0 *Store in a dry, dark, cool place |
| Special Storage Condition, Specify | Between 0 and 0 *Store in a dry, dark, cool place |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 08717648124075 [Primary] |
| GS1 | 28717648124079 [Package] Contains: 08717648124075 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 | 3 |
| Public Version Date | 2024-10-28 |
| Device Publish Date | 2016-02-05 |
| 28717648124079 - LOC | 2024-10-28.035 LOC Guide Wire Extension |
| 28717648124079 - LOC | 2024-10-28 .035 LOC Guide Wire Extension |
| 08717648356674 - Xact™ | 2024-10-28 Xact™ Transcarotid Stent System 9.0 mm x 40 mm Tapered |
| 08717648356681 - Xact™ | 2024-10-28 Xact™ Transcarotid Stent System 9.0 mm x 30 mm Tapered |
| 08717648356698 - Xact™ | 2024-10-28 Xact™ Transcarotid Stent System 9.0 mm x 30 mm Straight |
| 08717648356711 - Xact™ | 2024-10-28 Xact™ Transcarotid Stent System 8.0 mm x 40 mm Tapered |
| 08717648356728 - Xact™ | 2024-10-28 Xact™ Transcarotid Stent System 8.0 mm x 30 mm Tapered |
| 08717648356735 - Xact™ | 2024-10-28 Xact™ Transcarotid Stent System 8.0 mm x 30 mm Straight |
| 08717648356759 - Xact™ | 2024-10-28 Xact™ Transcarotid Stent System 7.0 mm x 30 mm Straight |