Primary Device ID | 16972130470453 |
NIH Device Record Key | 326922ed-e2e5-4ca9-b1c7-80fe3076f8ae |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | SmartPulse |
Version Model Number | 201-04-00 |
Company DUNS | 554507451 |
Company Name | Apex (Suzhou) Medical Products Company |
Device Count | 10 |
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 | false |
Expiration Date | true |
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 |
---|---|
GS1 | 16972130470453 [Unit of Use] |
GS1 | 26972130470450 [Primary] |
FQH | Lavage, Jet |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-11-04 |
Device Publish Date | 2020-10-27 |
16972130470453 | Apexpulse Hip Kit |
16972130470446 | Apexpulse Knee Kit |
06972130470456 | Apexpulse Hip Kit |
06972130470449 | Apexpulse Knee Kit |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() SMARTPULSE 88946041 not registered Live/Pending |
Carfield, Jonathan Ray 2020-06-03 |
![]() SMARTPULSE 85435173 4200012 Dead/Cancelled |
Dialog Semiconductor GmbH 2011-09-29 |
![]() SMARTPULSE 85434115 4764811 Live/Registered |
CYMER, LLC 2011-09-28 |
![]() SMARTPULSE 79379368 not registered Live/Pending |
SMARTPULSE TEKNOLOJI A.S. 2023-03-17 |
![]() SMARTPULSE 78322402 not registered Dead/Abandoned |
Galaxy Power, Inc. 2003-11-03 |
![]() SMARTPULSE 77529059 not registered Dead/Abandoned |
Oxypulse Medical Equipment Inc. 2008-07-23 |
![]() SMARTPULSE 75128664 2603254 Dead/Cancelled |
EL.EN.S.P.A. 1996-06-06 |