Primary Device ID | 00673978130415 |
NIH Device Record Key | a4fdecf1-aceb-4d73-abe8-21a557b2e392 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | GDLH® Posterior Spinal System |
Version Model Number | X0196-118 |
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 | |
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 |
Outer Diameter | 5.5 Millimeter |
Outer Diameter | 5.5 Millimeter |
Outer Diameter | 5.5 Millimeter |
Outer Diameter | 5.5 Millimeter |
Length | 18 Centimeter |
Outer Diameter | 5.5 Millimeter |
Length | 18 Centimeter |
Outer Diameter | 5.5 Millimeter |
Length | 18 Centimeter |
Outer Diameter | 5.5 Millimeter |
Length | 18 Centimeter |
Outer Diameter | 5.5 Millimeter |
Length | 18 Centimeter |
Outer Diameter | 5.5 Millimeter |
Length | 18 Centimeter |
Outer Diameter | 5.5 Millimeter |
Length | 18 Centimeter |
Outer Diameter | 5.5 Millimeter |
Length | 18 Centimeter |
Outer Diameter | 5.5 Millimeter |
Length | 18 Centimeter |
Outer Diameter | 5.5 Millimeter |
Length | 18 Centimeter |
Outer Diameter | 5.5 Millimeter |
Length | 18 Centimeter |
Outer Diameter | 5.5 Millimeter |
Length | 18 Centimeter |
Outer Diameter | 5.5 Millimeter |
Length | 18 Centimeter |
Outer Diameter | 5.5 Millimeter |
Length | 18 Centimeter |
Outer Diameter | 5.5 Millimeter |
Length | 18 Centimeter |
Outer Diameter | 5.5 Millimeter |
Length | 18 Centimeter |
Outer Diameter | 5.5 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00673978130415 [Primary] |
MNH | Orthosis, spondylolisthesis spinal fixation |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00673978130415]
Moist Heat or Steam Sterilization
[00673978130415]
Moist Heat or Steam Sterilization
[00673978130415]
Moist Heat or Steam Sterilization
[00673978130415]
Moist Heat or Steam Sterilization
[00673978130415]
Moist Heat or Steam Sterilization
[00673978130415]
Moist Heat or Steam Sterilization
[00673978130415]
Moist Heat or Steam Sterilization
[00673978130415]
Moist Heat or Steam Sterilization
[00673978130415]
Moist Heat or Steam Sterilization
[00673978130415]
Moist Heat or Steam Sterilization
[00673978130415]
Moist Heat or Steam Sterilization
[00673978130415]
Moist Heat or Steam Sterilization
[00673978130415]
Moist Heat or Steam Sterilization
[00673978130415]
Moist Heat or Steam Sterilization
[00673978130415]
Moist Heat or Steam Sterilization
[00673978130415]
Moist Heat or Steam Sterilization
[00673978130415]
Moist Heat or Steam Sterilization
[00673978130415]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2015-08-24 |
00673978130422 | ROD 5.5X20CM HEX TI |
00673978130415 | ROD 5.5X18CM HEX SS |
00673978130408 | ROD 5.5X16CM HEX SS |
00673978130392 | ROD 5.5X14CM HEX TI |
00673978130385 | ROD 5.5X12CM HEX TI |
00673978130361 | ROD 5.5X9CM HEX TI |
00673978130347 | ROD 5.5X7CM HEX TI |
00673978130316 | ROD 5.5X4CM HEX TI |
00673978130163 | TSR TT T-BOLT 14MM 5.5 TI |
00673978061825 | ROD 855-011 5.5 MM HEX-END ROD L20 TI |
00673978056258 | ROD 845-011 5.5MM HEX END L20 51CM |
00721902975233 | ROD 5.5X30CM-TI-HEX |
00721902975226 | ROD 5.5X28CM-TI-HEX |
00721902975219 | ROD 5.5X26CM-TI-HEX |
00721902975189 | ROD 5.5X22CM-TI-HEX |
00721902975158 | ROD 5.5X11CM-TI-HEX |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
GDLH 74476637 1998558 Dead/Cancelled |
SDGI HOLDINGS, INC. 1994-01-05 |