MULTI-LINK ULTRA 1003392-38
GUDID 08717648035494
MULTI-LINK OTW ULTRA Coronary Stent System 5.00 mmx 38 mm
ABBOTT VASCULAR INC.
Bare-metal coronary artery stent| Primary Device ID | 08717648035494 |
| NIH Device Record Key | 6965d971-c8e6-442a-bcf6-b0c9dfc05ca2 |
| Commercial Distribution Discontinuation | 2017-07-21 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | MULTI-LINK ULTRA |
| Version Model Number | 1003392-38 |
| Catalog Number | 1003392-38 |
| Company DUNS | 964569052 |
| Company Name | ABBOTT VASCULAR INC. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Conditional |
| 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
| 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 |
Operating and Storage Conditions
| 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. |
| 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 Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 08717648035494 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Approval: P970020
FDA Product Code
| MAF | STENT, CORONARY |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2019-10-07 |
| Device Publish Date | 2014-11-21 |
On-Brand Devices [MULTI-LINK ULTRA]
| 08717648035494 | MULTI-LINK OTW ULTRA Coronary Stent System 5.00 mmx 38 mm |
| 08717648035487 | MULTI-LINK OTW ULTRA Coronary Stent System 5.00 mm x 28 mm |
| 08717648035470 | MULTI-LINK OTW ULTRA Coronary Stent System 5.00 mm x 18 mm |
| 08717648035463 | MULTI-LINK OTW ULTRA Coronary Stent System 5.00 mm x 13 mm |
| 08717648035456 | MULTI-LINK OTW ULTRA Coronary Stent System 4.50 mm x 38 mm |
| 08717648035449 | MULTI-LINK OTW ULTRA Coronary Stent System 4.50 mm x 28 mm |
| 08717648035432 | MULTI-LINK OTW ULTRA Coronary Stent System 4.50 mm x 18 mm |
| 08717648035425 | MULTI-LINK OTW ULTRA Coronary Stent System 4.50 mm x 13 mm |
| 08717648035333 | MULTI-LINK RX ULTRA Coronary Stent System 5.00 mm x 38 mm |
| 08717648035326 | MULTI-LINK RX ULTRA Coronary Stent System 5.00 mm x 28 mm |
| 08717648035319 | MULTI-LINK RX ULTRA Coronary Stent System 5.00 mm x 18 mm |
| 08717648035302 | MULTI-LINK RX ULTRA Coronary Stent System 5.00 mm x 13 mm |
| 08717648035296 | MULTI-LINK RX ULTRA Coronary Stent System 4.50 mm x 38 mm |
| 08717648035289 | MULTI-LINK RX ULTRA Coronary Stent System 4.50 mm x 28 mm |
| 08717648035272 | MULTI-LINK RX ULTRA Coronary Stent System 4.50 mm x 18 mm |
| 08717648035265 | MULTI-LINK RX ULTRA Coronary Stent System 4.50 mm x 13 mm |
Trademark Results [MULTI-LINK ULTRA]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 MULTI-LINK ULTRA 77436941 3644610 Dead/Cancelled |
Abbott Cardiovascular Systems Inc. 2008-04-01 |
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