| Primary Device ID | 00612649111858 |
| NIH Device Record Key | 5abf785f-cd20-4d91-b798-ff187156f1bc |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | SAMPLE PORT ELBOW |
| Version Model Number | 7000 |
| Catalog Number | 7000 |
| Company DUNS | 009299017 |
| Company Name | King Systems Corporation |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| 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 | true |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00612649111858 [Package] Contains: 00612649190907 Package: [100 Units] In Commercial Distribution |
| GS1 | 00612649190907 [Primary] |
| CAI | Circuit, breathing (w connector, adaptor, y piece) |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-10-29 |
| Device Publish Date | 2020-10-21 |
| 00612649111858 | Elbow w/Tethered Cap |
| 00612649200620 | SAMPLE PORT ELBOW W/INJECTION CAP |
| 00612649200422 | SAMPLE PORT ELBOW |
| 00612649147246 | Tethered Elbow w/Red Cap |