UNIVERSAL F® FLEX® F92103
GUDID 00612649215990
UNIVERSAL F FLEX2 CIRCUIT & PACK KIT
King Systems Corporation
Anaesthesia breathing circuit, single-use| Primary Device ID | 00612649215990 |
| NIH Device Record Key | 8a22d4a4-5d58-4f09-af6a-d8bb374ce6ea |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | UNIVERSAL F® FLEX® |
| Version Model Number | F92103 |
| Catalog Number | F92103 |
| 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 | true |
| 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 | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
Customer Support Contacts
Device Dimensions
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00612649215990 [Package] Contains: 00612649216003 Package: [30 Units] In Commercial Distribution |
| GS1 | 00612649216003 [Primary] |
FDA Product Code
| CAI | Circuit, breathing (w connector, adaptor, y piece) |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | false |
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2022-09-14 |
| Device Publish Date | 2022-09-06 |
Devices Manufactured by King Systems Corporation
| 00612649217215 - PEDIATRIC ULTRA FLEX® | 2025-05-19 BREATHING CIRCUIT |
| 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 |
Trademark Results [UNIVERSAL F]
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 |
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