| Primary Device ID | 20860936000338 |
| NIH Device Record Key | 18537c01-a428-4db1-ab82-746fcba43c3d |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Luer Lock Set, Single Lumen |
| Version Model Number | LL0002 |
| Company DUNS | 022465035 |
| Company Name | THERMEDX, LLC |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Unsafe |
| 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 | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Pressure | 250 millibar |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00860936000334 [Primary] |
| GS1 | 20860936000338 [Package] Contains: 00860936000334 Package: Box [10 Units] In Commercial Distribution |
| HRX | Arthroscope |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-09-23 |
| 00860936000310 - Fluid Management System | 2018-07-06 |
| 00860936000327 - Fluid Management System | 2018-07-06 |
| 20860936000338 - Luer Lock Set, Single Lumen | 2018-07-06 |
| 20860936000338 - Luer Lock Set, Single Lumen | 2018-07-06 |
| 20860936000345 - High Pressure Luer Lock Set, Single Lumen 300mmHg | 2018-07-06 |
| 20860936000352 - Tubing Set - Single Lumen, Inflow with Dual Outflow | 2018-07-06 |
| 20860936000369 - Urology Set | 2018-07-06 Urology Set |