Primary Device ID | 00612649128108 |
NIH Device Record Key | 1085432d-dfe9-4e9d-bdc2-f9454c1a231f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | UNIVERSAL F® |
Version Model Number | U060-61 |
Catalog Number | U060-61 |
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 | 00612649128108 [Package] Contains: 00612649207735 Package: [30 Units] In Commercial Distribution |
GS1 | 00612649207735 [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 |