Primary Device ID | 00721902319792 |
NIH Device Record Key | 545bd0fa-c8fc-47a0-ad2a-85941159c8df |
Commercial Distribution Discontinuation | 2018-10-08 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | UCSS® Screw Set |
Version Model Number | 9098558 |
Company DUNS | 830350380 |
Company Name | MEDTRONIC SOFAMOR DANEK, 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 |
Length | 58 Millimeter |
Length | 58 Millimeter |
Length | 58 Millimeter |
Length | 58 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00721902319792 [Primary] |
MRW | SYSTEM, FACET SCREW SPINAL DEVICE |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00721902319792]
Moist Heat or Steam Sterilization
[00721902319792]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2019-01-25 |
Device Publish Date | 2015-07-30 |
00613994264237 | SCREW X10043510 TI 3.5X10MM THRPST |
00673978067971 | BONE SCREW 873-150 4.0 CAN CORT LAG L 50 |
00673978067964 | BONE SCREW 873-148 4.0 CAN CORT LAG L 48 |
00673978067957 | BONE SCREW 873-146 4.0 CAN CORT LAG L 46 |
00673978067940 | BONE SCREW 873-144 4.0 CAN CORT LAG L 44 |
00673978067933 | BONE SCREW 873-142 4.0 CAN CORT LAG L 42 |
00673978067926 | BONE SCREW 873-140 4.0 CAN CORT LAG L 40 |
00673978067919 | BONE SCREW 873-138 4.0 CAN CORT LAG L 38 |
00673978067902 | BONE SCREW 873-136 4.0 CAN CORT LAG L 36 |
00673978067896 | BONE SCREW 873-050 4.0 CANN CORT L 50MM |
00673978067889 | BONE SCREW 873-048 4.0 CANN CORT L 48MM |
00673978067872 | BONE SCREW 873-046 4.0 CANN CORT L 46MM |
00673978067865 | BONE SCREW 873-044 4.0 CANN CORT L 44MM |
00673978067858 | BONE SCREW 873-042 4.0 CANN CORT L 42MM |
00673978067841 | BONE SCREW 873-040 4.0 CANN CORT L 40MM |
00673978067834 | BONE SCREW 873-038 4.0 CANN CORT L 38MM |
00673978067827 | BONE SCREW 873-036 4.0 CANN CORT L 36MM |
00673978067810 | BONE SCREW 873-034 4.0 CANN CORT L 34MM |
00673978067803 | BONE SCREW 873-032 4.0 CANN CORT L 32MM |
00673978067797 | BONE SCREW 873-030 4.0 CANN CORT L 30MM |
00721902613371 | UCS DBLTHDSCR-TI-CANN-4.0X40 |
00721902319815 | 4.0 CORTICAL BONE SCREW 60MM |
00721902319792 | 4.0 CORTICAL BONE SCREW 58MM |
00721902319785 | 4.0 CORTICAL BONE SCREW 56MM |
00721902319778 | 4.0 CORTICAL BONE SCREW 54MM |
00721902319747 | 4.0 CORTICAL BONE SCREW 52MM |
00721902319730 | 4.0 CORTICAL BONE SCREW 50MM |
00721902319709 | 4.0 CORTICAL BONE SCREW 48MM |
00721902319693 | 4.0 CORTICAL BONE SCREW 46MM |
00721902319686 | 4.0 CORTICAL BONE SCREW 44MM |
00721902319679 | 4.0 CORTICAL BONE SCREW 42MM |
00721902319655 | 4.0 CORTICAL BONE SCREW 40MM |
00721902319617 | 4.0 CORTICAL BONE SCREW 38MM |
00721902319532 | 4.0 CORTICAL BONE SCREW 34MM |
00721902319518 | 4.0 CORTICAL BONE SCREW 30MM |
00721902319495 | 4.0 CORTICAL BONE SCREW 26MM |
00673978067759 | CASE 873-012 UCSS INSTRUMENT MODULE |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
UCSS 78357555 2974437 Live/Registered |
WARSAW ORTHOPEDIC, INC. 2004-01-26 |
UCSS 75557936 not registered Dead/Abandoned |
SDGI Holdings, Inc. 1998-09-23 |