| Primary Device ID | 00847536027060 |
| NIH Device Record Key | 51c274b3-6f11-4ee1-8869-477654c296bc |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | SolitaireTM |
| Version Model Number | SFR3-6-24-06 |
| Company DUNS | 826110710 |
| Company Name | Micro Therapeutics, 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 | false |
| 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)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com |
| Special Storage Condition, Specify | Between 0 and 0 *Store in a dry, cool place |
| Special Storage Condition, Specify | Between 0 and 0 *Store in a dry, cool place |
| Special Storage Condition, Specify | Between 0 and 0 *Store in a dry, cool place |
| Special Storage Condition, Specify | Between 0 and 0 *Store in a dry, cool place |
| Special Storage Condition, Specify | Between 0 and 0 *Store in a dry, cool place |
| Special Storage Condition, Specify | Between 0 and 0 *Store in a dry, cool place |
| Special Storage Condition, Specify | Between 0 and 0 *Store in a dry, cool place |
| Special Storage Condition, Specify | Between 0 and 0 *Store in a dry, cool place |
| Special Storage Condition, Specify | Between 0 and 0 *Store in a dry, cool place |
| Special Storage Condition, Specify | Between 0 and 0 *Store in a dry, cool place |
| Special Storage Condition, Specify | Between 0 and 0 *Store in a dry, cool place |
| Special Storage Condition, Specify | Between 0 and 0 *Store in a dry, cool place |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00847536027060 [Primary] |
| NRY | CATHETER, THROMBUS RETRIEVER |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2018-12-12 |
| Device Publish Date | 2017-09-24 |
| 00847536027060 | STENT SFR3-6-24-06 V01 |
| 00847536027053 | STENT SFR3-4-20-05 V01 |
| 00847536020559 | STENT SFR3-6-40-10V01 US |
| 00847536020542 | STENT SFR3-6-20-10V01 US |
| 00847536020535 | STENT SFR3-4-40-10V01 US |
| 00847536020528 | STENT SFR3-4-20-10V01 US |