| Primary Device ID | 10842289100791 |
| NIH Device Record Key | 19167579-8e82-4719-93b8-fe44a91cdc26 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Medisystems OneSite dual lumen buttonhole needle with steripick |
| Version Model Number | DL-2014PE |
| Company DUNS | 061310132 |
| Company Name | MEDISYSTEMS CORPORATION |
| 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 | 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 | 1-866-697-8243 |
| info@nxstage.com |
| Needle Gauge | 14 Gauge |
| Needle Gauge | 14 Gauge |
| Storage Environment Temperature | Between 0 Degrees Celsius and 40 Degrees Celsius |
| Storage Environment Temperature | Between 0 Degrees Celsius and 40 Degrees Celsius |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00842289100794 [Primary] |
| GS1 | 10842289100791 [Package] Contains: 00842289100794 Package: [150 Units] In Commercial Distribution |
| FIE | Needle, Fistula |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2018-03-29 |
| Device Publish Date | 2016-09-16 |
| 10842289100791 | DL-2014PE |
| 10842289100777 | DL-2004PE |
| 10842289100753 | DL-1214PE |
| 10842289100739 | DL-1204PE |