Primary Device ID | B741HA0 |
NIH Device Record Key | b41e8e2d-a50e-46b5-8342-8a7d596ada56 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Flotec |
Version Model Number | Hose Assembly |
Company DUNS | 103643730 |
Company Name | FLOTEC INC |
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 | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
HIBCC | B741HA0 [Primary] |
BYX | Tubing, Pressure And Accessories |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2021-10-15 |
Device Publish Date | 2021-10-07 |
B741RW0 | RW Regulator |
B741MC0 | Mass Casualty Assembly |
B741FM0 | Flowmeter |
B741DL0 | InGage Regulator |
B741HA0 | Hose Assembly |
B741CH0 | Hose Assembly - Canadian Standard |
B741TCB0 | T.O.A.D. Connection Box |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
FLOTEC 86575482 4845267 Live/Registered |
Flotec, Inc. 2015-03-25 |
FLOTEC 79057474 3692710 Dead/Cancelled |
BB IPR Limited 2008-04-25 |
FLOTEC 77372162 not registered Dead/Abandoned |
Glaxo Group Limited 2008-01-15 |
FLOTEC 75201083 2286910 Live/Registered |
PENTAIR FLOW TECHNOLOGIES, LLC 1996-11-20 |
FLOTEC 74418120 not registered Dead/Abandoned |
CIBA-GEIGY CORPORATION 1993-07-29 |
FLOTEC 74126205 not registered Dead/Abandoned |
Glaxo Group Limited 1990-12-21 |
FLOTEC 73286741 1195014 Dead/Cancelled |
Flotec Incorporated 1980-11-21 |