Primary Device ID | 07613327405866 |
NIH Device Record Key | 22725e86-1d49-43db-9d49-0f5de4be05dd |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | FlowPort |
Version Model Number | CAT02439 |
Catalog Number | CAT02439 |
Company DUNS | 187502109 |
Company Name | STRYKER CORPORATION |
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 | 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 | true |
OTC Over-The-Counter | false |
Phone | +1(866)624-4422 |
xx@xx.xx |
Device Issuing Agency | Device ID |
---|---|
GS1 | 07613327405866 [Primary] |
NBH | Accessories, arthroscopic |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2018-08-20 |
Device Publish Date | 2018-07-20 |
07613327405866 | FlowPort II Cannula with Obturator, Arthrex |
07613327405859 | FLOWPORT II ADAPTER, ARTHREX |
07613252633181 | FLOWPORT II CANNULA WITH OBTURATOR STRYKER 165MM |
07613252633051 | FLOWPORT II CANNULA WITH OBTURATOR LINVATEC AND STORZ |
07613252633037 | FLOWPORT II CANNULA WITH OBTURATOR STRYKER |
07613252632887 | FLOWPORT II CANNULA WITH OBTUR |
07613252632931 | CAT01030 |
07613252632917 | CAT00778 |
07613252632900 | CAT00777 |
07613252632894 | CAT00779 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() FLOWPORT 78922725 not registered Dead/Abandoned |
InnerSpace, Inc. 2006-07-05 |
![]() FLOWPORT 77838463 3908959 Live/Registered |
STRYKER CORPORATION 2009-09-30 |
![]() FLOWPORT 75801467 2628709 Dead/Cancelled |
Xerox Corporation 1999-09-17 |