Primary Device ID | 00763000713119 |
NIH Device Record Key | 45be702d-a55c-43f6-b38f-d526a20608a5 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ModuLeX™ Shank Mount |
Version Model Number | 9736437 |
Company DUNS | 835233107 |
Company Name | MEDTRONIC NAVIGATION, 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 | false |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00763000713119 [Primary] |
OLO | Orthopedic stereotaxic instrument |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00763000713119]
Moist Heat or Steam Sterilization
[00763000713119]
Moist Heat or Steam Sterilization
[00763000713119]
Moist Heat or Steam Sterilization
[00763000713119]
Moist Heat or Steam Sterilization
[00763000713119]
Moist Heat or Steam Sterilization
[00763000713119]
Moist Heat or Steam Sterilization
[00763000713119]
Moist Heat or Steam Sterilization
[00763000713119]
Moist Heat or Steam Sterilization
[00763000713119]
Moist Heat or Steam Sterilization
[00763000713119]
Moist Heat or Steam Sterilization
[00763000713119]
Moist Heat or Steam Sterilization
[00763000713119]
Moist Heat or Steam Sterilization
[00763000713119]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2025-07-28 |
Device Publish Date | 2025-07-19 |
00763000713126 | MODULEX SHANK MOUNT RIGHT 9736438 |
00763000713119 | MODULEX SHANK MOUNT LEFT 9736437 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() MODULEX 88911657 not registered Live/Pending |
WARSAW ORTHOPEDIC, INC. 2020-05-12 |
![]() MODULEX 79309623 not registered Live/Pending |
The Product Makers (Australia) Pty Limited 2020-09-24 |
![]() MODULEX 78914223 3451320 Live/Registered |
UNICAL AG S.P.A. 2006-06-22 |
![]() MODULEX 76515852 3181296 Live/Registered |
MODULEX INC. 2003-05-21 |
![]() MODULEX 74505041 1916317 Dead/Cancelled |
Computerized Medical Systems, Inc. 1994-03-25 |
![]() MODULEX 74385203 1827226 Dead/Expired |
FLEETWOOD SYSTEMS, INC. 1993-04-28 |
![]() MODULEX 73405892 1343780 Live/Registered |
A/S MODULEX 1982-12-13 |
![]() MODULEX 73193269 not registered Dead/Abandoned |
FEDOR EXPOSITIONS, INC. 1978-11-14 |
![]() MODULEX 73101282 1065780 Dead/Cancelled |
Modular Fixtures Corporation 1976-09-27 |
![]() MODULEX 73045750 1086248 Dead/Expired |
A/S MODULEX 1975-03-04 |
![]() MODULEX 72178295 0794016 Dead/Expired |
A/S MODULEX 1963-10-03 |
![]() MODULEX 72145854 0745172 Dead/Expired |
RITTER COMPANY, INC. 1962-05-31 |