REPEATER H93862
GUDID 50085412476686
REPEATER Pump Fluid Transfer Tube Set, Sterile, Std Volume, Bifurcated Sets
BAXTER CORPORATION ENGLEWOOD
Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose| Primary Device ID | 50085412476686 |
| NIH Device Record Key | 54822cf5-bfff-4440-9764-8dda1028bd05 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | REPEATER |
| Version Model Number | H93862 |
| Catalog Number | H93862 |
| 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 |
Customer Support Contacts
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00085412476681 [Primary] |
| GS1 | 50085412476686 [Package] Contains: 00085412476681 Package: CASE [10 Units] In Commercial Distribution |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K062909
FDA Product Code
| FPA | Set, administration, intravascular |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-09-23 |
On-Brand Devices [REPEATER]
| 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 |
Trademark Results [REPEATER]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 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 |
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.