| Primary Device ID | 00860008802064 |
| NIH Device Record Key | 47e7d9c5-d3a9-4bae-aefd-75b795c0f849 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ACCUSYNC |
| Version Model Number | 4200-3 |
| Catalog Number | 4200-3 |
| Company DUNS | 060000759 |
| Company Name | Accusync Medical Research Corporation |
| Device Count | 1 |
| DM Exempt | true |
| 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 | false |
| Serial Number | true |
| Manufacturing Date | true |
| 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 |
| Phone | 203-877-1610 |
| SALES@ACCUSYNC.COM | |
| Phone | 203-877-1610 |
| SALES@ACCUSYNC.COM | |
| Phone | 203-877-1610 |
| SALES@ACCUSYNC.COM | |
| Phone | 203-877-1610 |
| SALES@ACCUSYNC.COM | |
| Phone | 203-877-1610 |
| SALES@ACCUSYNC.COM | |
| Phone | 203-877-1610 |
| SALES@ACCUSYNC.COM | |
| Phone | 203-877-1610 |
| SALES@ACCUSYNC.COM | |
| Phone | 203-877-1610 |
| SALES@ACCUSYNC.COM | |
| Phone | 203-877-1610 |
| SALES@ACCUSYNC.COM | |
| Phone | 203-877-1610 |
| SALES@ACCUSYNC.COM | |
| Phone | 203-877-1610 |
| SALES@ACCUSYNC.COM | |
| Phone | 203-877-1610 |
| SALES@ACCUSYNC.COM | |
| Phone | 203-877-1610 |
| SALES@ACCUSYNC.COM | |
| Phone | 203-877-1610 |
| SALES@ACCUSYNC.COM | |
| Phone | 203-877-1610 |
| SALES@ACCUSYNC.COM | |
| Phone | 203-877-1610 |
| SALES@ACCUSYNC.COM | |
| Phone | 203-877-1610 |
| SALES@ACCUSYNC.COM |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00860008802064 [Primary] |
| IYY | Synchronizer, Electrocardiograph, Nuclear |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-11-18 |
| Device Publish Date | 2024-11-08 |
| 00860008802064 | ACCUSYNC 42 3 LEAD CARDIAC TRIGGER |
| 00860008802057 | ACCUSYNC 72 5 LEAD CARDIAC TRIGGER MONITOR WITH PRINTER OPTION |
| 00860008802033 | ACCUSYNC 72 3 LEAD CARDIAC TRIGGER MONITOR WITH PRINTER OPTION |
| 00860008802026 | ACCUSYNC 72 3-LEAD CARDIAC TRIGGER SYSTEM |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() ACCUSYNC 87845573 5606078 Live/Registered |
NEC DISPLAY SOLUTIONS, LTD. 2018-03-22 |
![]() ACCUSYNC 85009263 3838167 Live/Registered |
FEI-Zyfer, Inc. 2010-04-08 |
![]() ACCUSYNC 76022271 not registered Dead/Abandoned |
Dunlop Maxfli Sports Corporation 2000-04-10 |
![]() ACCUSYNC 75744783 not registered Dead/Abandoned |
NEC Technologies, Inc. 1999-07-07 |
![]() ACCUSYNC 75714007 2601624 Dead/Expired |
LPS IP HOLDING COMPANY, LLC 1999-05-26 |
![]() ACCUSYNC 75692041 2348491 Dead/Cancelled |
Sturdy Corporation 1999-04-26 |
![]() ACCUSYNC 75520997 2259579 Dead/Cancelled |
FEI-ZYFER, INC. 1998-07-07 |
![]() ACCUSYNC 74576927 1959836 Live/Registered |
ACCUSYNC MEDICAL RESEARCH CORP. 1994-09-22 |