Primary Device ID | 03662663046978 |
NIH Device Record Key | 9ef44625-2926-48ba-a922-3fc6f3d9dd80 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ROI-A |
Version Model Number | SI-ROIA-0024 |
Catalog Number | SI-ROIA-0024 |
Company DUNS | 615789729 |
Company Name | LDR Spine Usa, 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 |
Phone | 800-699-3360 |
custserv@ldrspine.com | |
Phone | 800-699-3360 |
custserv@ldrspine.com | |
Phone | 800-699-3360 |
custserv@ldrspine.com | |
Phone | 800-699-3360 |
custserv@ldrspine.com | |
Phone | 800-699-3360 |
custserv@ldrspine.com | |
Phone | 800-699-3360 |
custserv@ldrspine.com | |
Phone | 800-699-3360 |
custserv@ldrspine.com | |
Phone | 800-699-3360 |
custserv@ldrspine.com | |
Phone | 800-699-3360 |
custserv@ldrspine.com | |
Phone | 800-699-3360 |
custserv@ldrspine.com | |
Phone | 800-699-3360 |
custserv@ldrspine.com | |
Phone | 800-699-3360 |
custserv@ldrspine.com | |
Phone | 800-699-3360 |
custserv@ldrspine.com | |
Phone | 800-699-3360 |
custserv@ldrspine.com | |
Phone | 800-699-3360 |
custserv@ldrspine.com | |
Phone | 800-699-3360 |
custserv@ldrspine.com | |
Phone | 800-699-3360 |
custserv@ldrspine.com | |
Phone | 800-699-3360 |
custserv@ldrspine.com | |
Phone | 800-699-3360 |
custserv@ldrspine.com | |
Phone | 800-699-3360 |
custserv@ldrspine.com | |
Phone | 800-699-3360 |
custserv@ldrspine.com | |
Phone | 800-699-3360 |
custserv@ldrspine.com | |
Phone | 800-699-3360 |
custserv@ldrspine.com | |
Phone | 800-699-3360 |
custserv@ldrspine.com | |
Phone | 800-699-3360 |
custserv@ldrspine.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 03662663046978 [Primary] |
OVD | Intervertebral Fusion Device With Integrated Fixation, Lumbar |
Steralize Prior To Use | true |
Device Is Sterile | false |
[03662663046978]
Moist Heat or Steam Sterilization
[03662663046978]
Moist Heat or Steam Sterilization
[03662663046978]
Moist Heat or Steam Sterilization
[03662663046978]
Moist Heat or Steam Sterilization
[03662663046978]
Moist Heat or Steam Sterilization
[03662663046978]
Moist Heat or Steam Sterilization
[03662663046978]
Moist Heat or Steam Sterilization
[03662663046978]
Moist Heat or Steam Sterilization
[03662663046978]
Moist Heat or Steam Sterilization
[03662663046978]
Moist Heat or Steam Sterilization
[03662663046978]
Moist Heat or Steam Sterilization
[03662663046978]
Moist Heat or Steam Sterilization
[03662663046978]
Moist Heat or Steam Sterilization
[03662663046978]
Moist Heat or Steam Sterilization
[03662663046978]
Moist Heat or Steam Sterilization
[03662663046978]
Moist Heat or Steam Sterilization
[03662663046978]
Moist Heat or Steam Sterilization
[03662663046978]
Moist Heat or Steam Sterilization
[03662663046978]
Moist Heat or Steam Sterilization
[03662663046978]
Moist Heat or Steam Sterilization
[03662663046978]
Moist Heat or Steam Sterilization
[03662663046978]
Moist Heat or Steam Sterilization
[03662663046978]
Moist Heat or Steam Sterilization
[03662663046978]
Moist Heat or Steam Sterilization
[03662663046978]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2022-03-10 |
Device Publish Date | 2017-03-23 |
03662663041782 | ROI-A REMOVAL DEVICE |
03662663047050 | ROI-A Simplified Implant Holder |
03662663047005 | ROI-A RADD Retention Rod |
03662663046992 | ROI-A RADD Implant Holder Shaft |
03662663046930 | ROI-A Cage Holder with Impaction Lines |
03662663046923 | ROI-A Minimal Holder |
03662663043090 | IR9433R |
03662663041768 | ROI-A MEDIAN IMPLANT HOLDER |
03662663041683 | ANCHORING PLATE HOLDER |
03662663046190 | IR992 |
03662663024365 | IR997 |
03662663047067 | ROI-A Awl Impactor with Impaction Lines |
03662663047043 | ROI-A Starter Trial |
03662663047036 | ROI-A RADD Plate Impactor - Short |
03662663047029 | ROI-A RADD Plate Impactor - Long |
03662663047012 | ROI-A RADD Impaction Handle |
03662663046985 | ROI-A RADD Distractor Blade Split |
03662663046978 | ROI-A RADD Distractor Blade Solid |
03662663046961 | ROI-A RADD Distractor Body |
03662663046954 | ROI-A Long Impactor with Impaction Lines |
03662663046947 | ROI-A Short Impactor with Impaction Lines |
03662663043113 | ROI-A ADJUSTABLE STOP |
03662663043106 | IR9434R |
03662663043083 | IR9432R |
03662663043076 | IR9431R |
03662663043069 | IR9430R |
03662663043021 | IR9409R |
03662663043007 | IR9407R |
03662663042994 | IR9405R |
03662663042987 | ROI-A TRIAL 33X36 H19 14° |
03662663042970 | ROI-A TRIAL 33X36 H18 14° |
03662663042963 | ROI-A TRIAL 33X36 H17 14° |
03662663042956 | ROI-A TRIAL 33X36 H16 14° |
03662663042949 | ROI-A TRIAL 33X36 H15 14° |
03662663042925 | ROI-A TRIAL 33X36 H14 14° |
03662663042918 | ROI-A TRIAL 33X36 H19 10° |
03662663042901 | ROI-A TRIAL 33X36 H18 10° |
03662663042895 | ROI-A TRIAL 33X36 H17 10° |
03662663042888 | ROI-A TRIAL 33X36 H16 10° |
03662663042871 | ROI-A TRIAL 33X36 H15 10° |
03662663042864 | ROI-A TRIAL 33X36 H14 10° |
03662663042857 | ROI-A TRIAL 33X36 H13 10° |
03662663042840 | ROI-A TRIAL 33X36 H12 10° |
03662663042833 | ROI-A TRIAL 33X36 H17 6° |
03662663042819 | ROI-A TRIAL 33X36 H16 6° |
03662663042802 | ROI-A TRIAL 33X36 H15 6° |
03662663042796 | ROI-A TRIAL 33X36 H14 6° |
03662663042789 | ROI-A TRIAL 33X36 H13 6° |
03662663042772 | ROI-A TRIAL 33X36 H12 6° |
03662663042765 | ROI-A TRIAL 33X36 H11 6° |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
ROI-A 77288505 3573548 Live/Registered |
ZIMMER BIOMET SPINE, INC. 2007-09-25 |