| Primary Device ID | 10813939024958 |
| NIH Device Record Key | 634fa931-d264-469d-aff8-f538b5481cff |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Gastrostomy Tube - Dual ENFit Port (Tri-Funnel) |
| Version Model Number | VED-222 |
| Catalog Number | 70-0062-222 |
| Company DUNS | 183325125 |
| Company Name | XERIDIEM MEDICAL DEVICES, 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 | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Phone | (520) 882-7794 |
| smurray@xeridiem.com | |
| Phone | (520) 882-7794 |
| smurray@xeridiem.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00813939024951 [Primary] |
| GS1 | 10813939024958 [Package] Contains: 00813939024951 Package: Case Box [5 Units] In Commercial Distribution |
| PIF | Gastrointestinal Tubes With Enteral Specific Connectors |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2019-10-07 |
| Device Publish Date | 2016-08-08 |
| 10813939024958 | Gastrostomy Tube - Dual ENFit Port (Tri-Funnel) 22FR |
| 10813939024941 | Gastrostomy Tube - Dual ENFit Port (Tri-Funnel) 20FR |
| 10813939024934 | Gastrostomy Tube - Dual ENFit Port (Tri-Funnel) 18FR |
| 10813939024927 | Gastrostomy Tube - Dual ENFit Port (Tri-Funnel) 16FR |
| 10813939024910 | Gastrostomy Tube - Dual ENFit Port (Tri-Funnel) 14FR |