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 |