UNIVERSAL F® FlexBREATHING CIRCUIT & PACK KIT F98003
GUDID 00612649213569
UNIVERSAL F FLEX CIRCUIT PACK KIT
King Systems Corporation
Anaesthesia breathing circuit, single-use| Primary Device ID | 00612649213569 |
| NIH Device Record Key | 1bbc3058-df02-4c06-b986-523def2f5a27 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | UNIVERSAL F® FlexBREATHING CIRCUIT & PACK KIT |
| Version Model Number | F98003 |
| Catalog Number | F98003 |
| 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 | true |
| 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 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 | 00612649213569 [Package] Contains: 00612649213576 Package: [50 Units] In Commercial Distribution |
| GS1 | 00612649213576 [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 | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2019-11-27 |
| Device Publish Date | 2019-01-29 |
On-Brand Devices [UNIVERSAL F® FlexBREATHING CIRCUIT & PACK KIT]
| 00612649213569 | UNIVERSAL F FLEX CIRCUIT PACK KIT |
| 00612649182261 | UNIVERSAL F FLEX PACK KIT 40/CS |
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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