Primary Device ID | 50085412476594 |
NIH Device Record Key | fc18f839-58e8-4991-bd34-fc619a4587f5 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | REPEATER |
Version Model Number | H93812 |
Catalog Number | H93812 |
Company DUNS | 078383477 |
Company Name | BAXTER CORPORATION ENGLEWOOD |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
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 | false |
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 |
Phone | +1(800)933-0303 |
Medinfo_medproducts@baxter.com | |
Phone | +1(800)933-0303 |
Medinfo_medproducts@baxter.com | |
Phone | +1(800)933-0303 |
Medinfo_medproducts@baxter.com | |
Phone | +1(800)933-0303 |
Medinfo_medproducts@baxter.com | |
Phone | +1(800)933-0303 |
Medinfo_medproducts@baxter.com | |
Phone | +1(800)933-0303 |
Medinfo_medproducts@baxter.com | |
Phone | +1(800)933-0303 |
Medinfo_medproducts@baxter.com | |
Phone | +1(800)933-0303 |
Medinfo_medproducts@baxter.com | |
Phone | +1(800)933-0303 |
Medinfo_medproducts@baxter.com | |
Phone | +1(800)933-0303 |
Medinfo_medproducts@baxter.com | |
Phone | +1(800)933-0303 |
Medinfo_medproducts@baxter.com | |
Phone | +1(800)933-0303 |
Medinfo_medproducts@baxter.com | |
Phone | +1(800)933-0303 |
Medinfo_medproducts@baxter.com | |
Phone | +1(800)933-0303 |
Medinfo_medproducts@baxter.com | |
Phone | +1(800)933-0303 |
Medinfo_medproducts@baxter.com | |
Phone | +1(800)933-0303 |
Medinfo_medproducts@baxter.com | |
Phone | +1(800)933-0303 |
Medinfo_medproducts@baxter.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00085412476599 [Primary] |
GS1 | 50085412476594 [Package] Contains: 00085412476599 Package: CASE [10 Units] In Commercial Distribution |
FMF | Syringe, piston |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-09-23 |
50085412477003 | REPEATER Pump Fluid Transfer Tube Set, Sterile, Std Volume, Low Priming |
50085412476846 | REPEATER Pump Extension Set, Male LL to Male LL |
50085412476693 | REPEATER Pump Fluid Transfer Tube Set, Sterile, Std Volume, Trifurcated |
50085412476686 | REPEATER Pump Fluid Transfer Tube Set, Sterile, Std Volume, Bifurcated Sets |
50085412476594 | REPEATER Pump Fluid Transfer Tube Set, Non-Vented Spike - Luer Lock |
50085412476549 | REPEATER Pump Universal Spike, Sterile, Luer Lock |
50085412476525 | REPEATER Pump Fluid Transfer Tube Set, Sterile, Std Volume, Luer Lock Ends |
50085412476518 | REPEATER Pump Fluid Transfer Tube Set, Non-Sterile |
50085412475726 | Sterile REPEATER Pump Tube Sets, Universal Spike - Luer Lock |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
REPEATER 98717621 not registered Live/Pending |
Repeater, Inc. 2024-08-26 |
REPEATER 87441557 5350148 Live/Registered |
Reverie Brewing Company, LLC 2017-05-09 |
REPEATER 86691049 4901464 Live/Registered |
Baxter Corporation Englewood 2015-07-13 |
REPEATER 85638774 4275343 Live/Registered |
BAXA CORPORATION 2012-05-30 |
REPEATER 75512911 2439823 Dead/Cancelled |
Compugen, Ltd. 1998-07-02 |
REPEATER 75271276 2279770 Dead/Cancelled |
Zircon Corporation 1997-04-07 |
REPEATER 75082534 2066795 Live/Registered |
EPPENDORF AG 1996-04-02 |
REPEATER 74801227 1789886 Dead/Cancelled |
Platte Chemical Co. 1991-04-19 |
REPEATER 74158864 not registered Dead/Abandoned |
Platte Chemical Co. 1991-04-19 |
REPEATER 73632039 1445347 Dead/Cancelled |
JOHN RILEY GOLF INC. 1986-11-24 |
REPEATER 73182818 1129349 Dead/Cancelled |
JOHN RILEY GOLF CO. 1978-08-21 |
REPEATER 71488458 0420422 Dead/Expired |
EVERSHARP, INC. 1945-09-14 |