| Primary Device ID | 00612649111926 |
| NIH Device Record Key | cd89e794-ca3f-4962-8526-db6036d95e9b |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | SAMPLE PORT T-PIECE |
| Version Model Number | 7018 |
| Catalog Number | 7018 |
| 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 | 00612649111926 [Package] Contains: 00612649190938 Package: [100 Units] In Commercial Distribution |
| GS1 | 00612649190938 [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 | 2021-06-14 |
| Device Publish Date | 2021-06-04 |
| 00612649216942 - UNIVERSAL FLEX2® | 2024-12-09 UNIVERSAL FLEX2 CIRCUIT |
| 00612649216966 - UNIVERSAL FLEX2®BREATHING CIRCUIT | 2024-12-09 UNIVERSAL FLEX2 CIRCUIT |
| 00612649216980 - UNIVERSAL FLEX2®BREATHING CIRCUIT | 2024-12-09 UNIVERSAL FLEX2 CIRCUIT |
| 00612649217000 - UNIVERSAL FLEX2® | 2024-12-09 UNIVERSAL FLEX2 CIRCUIT |
| 00612649217024 - UNIVERSAL FLEX2® | 2024-12-09 UNIVERSAL FLEX2 CIRCUIT |
| 00612649217048 - UNIVERSAL FLEX2® | 2024-12-09 UNIVERSAL FLEX2 CIRCUIT |
| 00612649217062 - UNIVERSAL FLEX2® | 2024-12-09 UNIVERSAL FLEX2 CIRCUIT |
| 00612649217086 - UNIVERSAL FLEX2® | 2024-12-09 UNIVERSAL FLEX2 CIRCUIT |