Primary Device ID | 00643169789630 |
NIH Device Record Key | adef600a-c32a-4495-9736-36a6926f6738 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Straightshot® M4 |
Version Model Number | 1898075 |
Company DUNS | 835465063 |
Company Name | MEDTRONIC XOMED, INC. |
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 | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00643169789630 [Primary] |
ERL | DRILL, SURGICAL, ENT (ELECTRIC OR PNEUMATIC) INCLUDING HANDPIECE |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 5 |
Public Version Date | 2019-08-09 |
Device Publish Date | 2017-04-16 |
00643169789630 | INSTRUMENT TRAY 1898075 M4 |
00763000172121 | INSTRUMENT TRAY 1898075 M4 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() STRAIGHTSHOT 85966970 not registered Dead/Abandoned |
North American Specialty Products LLC 2013-06-21 |
![]() STRAIGHTSHOT 85829013 4472379 Live/Registered |
NORTH AMERICAN SPECIALTY PRODUCTS LLC 2013-01-22 |
![]() STRAIGHTSHOT 78678959 3288807 Live/Registered |
NABORS DRILLING TECHNOLOGIES USA, INC. 2005-07-26 |
![]() STRAIGHTSHOT 75652661 not registered Dead/Abandoned |
Heartport, Inc 1999-03-03 |
![]() STRAIGHTSHOT 75154044 2114841 Live/Registered |
Medtronic Xomed, Inc. 1996-08-19 |
![]() STRAIGHTSHOT 73358781 not registered Dead/Abandoned |
JODY MELTEBEKE, SCOTT STAFFORD, MARKSTAFFORD, MICHAEL MORGAN, AND LAURASYLVESTER 1982-04-08 |