| Primary Device ID | 00847536020160 |
| NIH Device Record Key | f83bb409-3b0d-4759-bed9-23980f08947d |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | CaptureTM |
| Version Model Number | 300015 |
| 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 | 00847536020160 [Primary] |
| NRY | CATHETER, THROMBUS RETRIEVER |
| Steralize Prior To Use | true |
| Device Is Sterile | true |
[00847536020160]
Ethylene Oxide
[00847536020160]
Ethylene Oxide
[00847536020160]
Ethylene Oxide
[00847536020160]
Ethylene Oxide
[00847536020160]
Ethylene Oxide
[00847536020160]
Ethylene Oxide
[00847536020160]
Ethylene Oxide
[00847536020160]
Ethylene Oxide
[00847536020160]
Ethylene Oxide
[00847536020160]
Ethylene Oxide
[00847536020160]
Ethylene Oxide
[00847536020160]
Ethylene Oxide
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-04-07 |
| 00847536020191 | 300018 CAPTURE LP 3X20 US |
| 00847536020184 | 300017 CAPTURE LP 4X20 US |
| 00847536020177 | 300016 CAPTURE LP 3X30 US |
| 00847536020160 | 300015 CAPUTRE LP 4X30 US |
| 00847536020153 | 300018 CAPTURE LP 3X20 US |
| 00847536020146 | 300017 CAPTURE LP 4X20 US |
| 00847536020139 | 300016 CAPTURE LP 3X30 US |
| 00847536020122 | 300015 CAPTURE LP 4X30 US |