| Primary Device ID | 08717648013317 |
| NIH Device Record Key | 75445ccd-e974-4d9f-824a-9c07e7f19514 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | DOC |
| Version Model Number | 22260 |
| Catalog Number | 22260 |
| 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 | |
| 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 *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 Issuing Agency | Device ID |
|---|---|
| GS1 | 08717648013317 [Primary] |
| GS1 | 28717648013311 [Package] 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 | 5 |
| Public Version Date | 2020-03-23 |
| Device Publish Date | 2016-02-05 |
| 08717648353765 - Esprit™ | 2025-07-21 Esprit™ BTK Everolimus Eluting Resorbable Scaffold System 3.75mm x 28mm Over-The-Wire |
| 08717648353666 - Esprit™ | 2025-07-18 Esprit™ BTK Everolimus Eluting Resorbable Scaffold System 3.50mm x 18mm Over-The-Wire |
| 08717648353680 - Esprit™ | 2025-07-18 Esprit™ BTK Everolimus Eluting Resorbable Scaffold System 3.50mm x 28mm Over-The-Wire |
| 08717648353703 - Esprit™ | 2025-07-18 Esprit™ BTK Everolimus Eluting Resorbable Scaffold System 3.50mm x 38mm Over-The-Wire |
| 08717648353741 - Esprit™ | 2025-07-18 Esprit™ BTK Everolimus Eluting Resorbable Scaffold System 3.75mm x 18mm Over-The-Wire |
| 08717648353789 - Esprit™ | 2025-07-18 Esprit™ BTK Everolimus Eluting Resorbable Scaffold System 3.75mm x 38mm Over-The-Wire |
| 08717648353826 - Esprit™ | 2025-07-18 Esprit™ BTK Everolimus Eluting Resorbable Scaffold System 2.50mm x 18mm Over-The-Wire |
| 08717648353840 - Esprit™ | 2025-07-18 Esprit™ BTK Everolimus Eluting Resorbable Scaffold System 2.50mm x 28mm Over-The-Wire |