| Primary Device ID | 00612649128054 |
| NIH Device Record Key | a9f037e7-f670-4518-b1f6-1799838102b5 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | UNIVERSAL F® |
| Version Model Number | U040-61 |
| Catalog Number | U040-61 |
| 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 | 00612649128054 [Package] Contains: 00612649207698 Package: [30 Units] In Commercial Distribution |
| GS1 | 00612649207698 [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 | 2021-03-31 |
| Device Publish Date | 2021-03-23 |
| 00612649128825 | UNIVERSAL F TRANSPORT KIT |
| 00612649128108 | UNIVERSAL F CIRCUIT |
| 00612649128054 | UNIVERSAL F CIRCUIT |
| 00612649128603 | UNIVERSAL F CIRCUIT |
| 00612649170510 | UNIVERSAL F CIRCUIT |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() UNIVERSAL F 74475379 1884793 Live/Registered |
KING SYSTEMS CORPORATION 1994-01-03 |
![]() UNIVERSAL F 74323503 not registered Dead/Abandoned |
King Systems- Division of Burco Molding, Inc. 1992-10-19 |