| Primary Device ID | 00847536041769 |
| NIH Device Record Key | add1a4d9-a2bf-4d71-bf1b-92d39cd1edf0 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | PhenomTM 17 Catheter |
| Version Model Number | FG11160-0615-2R |
| Company DUNS | 826110710 |
| Company Name | Micro Therapeutics, 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 | 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 |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight Keep Dry |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00847536041769 [Primary] |
| KRA | Catheter, continuous flush |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2019-04-30 |
| Device Publish Date | 2019-04-22 |
| 00847536041783 | CATHETER FG11160-0615-2X V04 |
| 00847536041776 | CATHETER FG11160-0615-2S V04 |
| 00847536041769 | CATHETER FG11160-0615-2R V04 |
| 00847536041752 | CATHETER FG11160-0615-2J V04 |
| 00847536041745 | CATHETER FG11160-0615-1S V04 |
| 00847536041738 | CATHETER FG11150-0615-2X V04 |
| 00847536041721 | CATHETER FG11150-0615-2S V04 |
| 00847536041714 | CATHETER FG11150-0615-2R V04 |
| 00847536041707 | CATHETER FG11150-0615-2J V04 |
| 00763000399672 | CATHETER FG11150-0615-2X V06 US |
| 00763000399665 | CATHETER FG11150-0615-2S V06 US |
| 00763000399658 | CATHETER FG11150-0615-2R V06 US |
| 00763000399641 | CATHETER FG11150-0615-2J V06 US |