| Primary Device ID | 00847536041882 |
| NIH Device Record Key | 1025ce72-d5c7-495f-9276-25bb6bed7026 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | PhenomTM 27 Catheter |
| Version Model Number | FG15160-0615-1S |
| 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 | 00847536041882 [Primary] |
| DQY | Catheter, percutaneous |
| 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 |
| 00847536041882 | CATHETER FG15160-0615-1S V04 |
| 00847536041875 | CATHETER FG15150-0630-1S V04 |
| 00847536041868 | CATHETER FG15150-0615-1S V04 |
| 00847536041851 | CATHETER FG15135-0615-1S V04 |
| 00763000399726 | CATHETER FG15160-0615-1S V06 US |
| 00763000399719 | CATHETER FG15150-0630-1S V06 US |
| 00763000399702 | CATHETER FG15150-0615-1S V06 US |