| Primary Device ID | 50810988021202 |
| NIH Device Record Key | 3c7410e0-9dd7-4412-be98-ad810ebdf8fa |
| Commercial Distribution Discontinuation | 2019-11-22 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | MEDCOMP GEN III POWER INJECTABLE PORT |
| Version Model Number | JT150806101 |
| Company DUNS | 079506014 |
| Company Name | JET MEDICAL, INC. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Conditional |
| Human Cell/Tissue Product | false |
| Device Kit | true |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Phone | +1(866)385-4047 |
| CUSTOMERSERVICE@JETMEDICALINC.COM | |
| Phone | +1(866)385-4047 |
| CUSTOMERSERVICE@JETMEDICALINC.COM |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00810988021207 [Primary] |
| GS1 | 50810988021202 [Package] Contains: 00810988021207 Package: BOX [5 Units] Discontinued: 2019-11-22 Not in Commercial Distribution |
| LJT | Port & Catheter, Implanted, Subcutaneous, Intravascular |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 6 |
| Public Version Date | 2019-12-05 |
| Device Publish Date | 2018-02-13 |
| 50810988021226 | 8F PLASTIC DURAPORT LOW PROFILE CT PORT W/ATTACHABLE CHRONOFLEX® POLYURETHANE CATHETER |
| 50810988021219 | 6.6F PLASTIC DURAPORT LOW PROFILE CT PORT W/ATTACHABLE CHRONOFLEX® POLYURETHANE CATHETER |
| 50810988021202 | 8F PLASTIC ELLIPTIPORT MID-SIZED CT PORT W/ATTACHABLE CHRONOFLEX® POLYURETHANE CATHETER |
| 50810988021196 | 6.6F PLASTIC ELLIPTIPORT MID-SIZED CT PORT W/ATTACHABLE CHRONOFLEX® POLYURETHANE CATHETER |