Primary Device ID | 00763000406073 |
NIH Device Record Key | 0d4b1c62-fc97-4ef4-8b9e-80046c9a36cb |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Becker |
Version Model Number | 46128 |
Company DUNS | 089055867 |
Company Name | MEDTRONIC PS MEDICAL, 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 | true |
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 |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00763000406073 [Primary] |
JXG | Shunt, central nervous system and components |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-04-08 |
Device Publish Date | 2024-03-31 |
00763000572921 | EDMS 27811 BECKER GRN PL VCATH |
00763000572877 | BECKER 27672 ONEWAY VLV Y-SITE PT LN |
00763000572839 | EDMS 24146 BECKER NO Y-SITE |
00763000529369 | KIT 25068 EDM 46124 46126 |
00763000529345 | EDMS 27779 BECKER BC NDLESS BOND CONN |
00763000529314 | BECKER 27670 STOP BELOW DC NDL-LS IN |
00763000529307 | BECKER 27609 W/NEEDLESLESS INJ. SITE |
00763000467326 | EDMS 27702 EURO BECKER II GR PT LN |
00763000431297 | EDMS II 25120 BECKER W/1-WAY VALVE |
00763000431259 | EDMS 46129 EURO BECKER II BLUE PT LN |
00763000406073 | EDMS 46128 BECKER II BLUE PT LN |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() BECKER 97784744 not registered Live/Pending |
Conleasco, Inc. 2023-02-07 |
![]() BECKER 88072578 not registered Live/Pending |
DELTA FAUCET COMPANY 2018-08-09 |
![]() BECKER 87587682 5568517 Live/Registered |
Becker Orthopedic Appliance Company 2017-08-29 |
![]() BECKER 87312951 5289805 Live/Registered |
CBS Studios Inc. 2017-01-25 |
![]() BECKER 87312937 5289803 Live/Registered |
CBS Studios Inc. 2017-01-25 |
![]() BECKER 87232005 5568050 Live/Registered |
Industrias Becker Ltda. 2016-11-09 |
![]() BECKER 85564980 4236880 Live/Registered |
Becker Law Office, PLC 2012-03-09 |
![]() BECKER 85413973 4141950 Dead/Cancelled |
Becker & Associates Consulting, Inc. 2011-09-02 |
![]() BECKER 79212996 not registered Live/Pending |
Gebr. Becker GmbH 2017-01-16 |
![]() BECKER 79014386 3159049 Dead/Cancelled |
Becker-Antriebe GmbH 2004-04-29 |
![]() BECKER 78788449 3297415 Live/Registered |
DRESSER LLC 2006-01-10 |
![]() BECKER 78471679 3072867 Live/Registered |
Medtronic, Inc. 2004-08-23 |