Primary Device ID | 03662663015974 |
NIH Device Record Key | 7be8b198-59ff-480a-a1a8-012cf1ee2de6 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ROI |
Version Model Number | IR504P |
Company DUNS | 615789729 |
Company Name | LDR Spine Usa, Inc. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Conditional |
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 | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Length | 24 Millimeter |
Height | 9 Millimeter |
Length | 24 Millimeter |
Height | 9 Millimeter |
Length | 24 Millimeter |
Height | 9 Millimeter |
Length | 24 Millimeter |
Height | 9 Millimeter |
Length | 24 Millimeter |
Height | 9 Millimeter |
Length | 24 Millimeter |
Height | 9 Millimeter |
Length | 24 Millimeter |
Height | 9 Millimeter |
Length | 24 Millimeter |
Height | 9 Millimeter |
Length | 24 Millimeter |
Height | 9 Millimeter |
Length | 24 Millimeter |
Height | 9 Millimeter |
Length | 24 Millimeter |
Height | 9 Millimeter |
Length | 24 Millimeter |
Height | 9 Millimeter |
Length | 24 Millimeter |
Height | 9 Millimeter |
Length | 24 Millimeter |
Height | 9 Millimeter |
Length | 24 Millimeter |
Height | 9 Millimeter |
Length | 24 Millimeter |
Height | 9 Millimeter |
Length | 24 Millimeter |
Height | 9 Millimeter |
Length | 24 Millimeter |
Height | 9 Millimeter |
Length | 24 Millimeter |
Height | 9 Millimeter |
Length | 24 Millimeter |
Height | 9 Millimeter |
Length | 24 Millimeter |
Height | 9 Millimeter |
Length | 24 Millimeter |
Height | 9 Millimeter |
Length | 24 Millimeter |
Height | 9 Millimeter |
Length | 24 Millimeter |
Height | 9 Millimeter |
Length | 24 Millimeter |
Height | 9 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 03662663015974 [Primary] |
MQP | Spinal Vertebral Body Replacement Device |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2022-03-10 |
Device Publish Date | 2015-10-24 |
03662663042499 | IR935R |
03662663043151 | IR946R |
03662663043144 | IR945R |
03662663042710 | IR937R |
03662663042604 | IR936R |
03662663041577 | IR913R |
03662663041492 | IR912R |
03662663046060 | IR990 |
03662663043137 | TRIAL IMPLANT 8° H14mm |
03662663043120 | TRIAL IMPLANT 8° H12mm |
03662663043052 | TRIAL IMPLANT 8° H10mm |
03662663043045 | TRIAL IMPLANT 5° H12mm |
03662663043038 | TRIAL IMPLANT 5° H10mm |
03662663042932 | TRIAL IMPLANT 0° H12mm |
03662663042826 | TRIAL IMPLANT 0° H10mm |
03662663042383 | TRIAL IMPLANT 8° H13mm |
03662663042277 | TRIAL IMPLANT 8° H11mm |
03662663042161 | TRIAL IMPLANT 8° H09mm |
03662663042055 | TRIAL IMPLANT 5° H13mm |
03662663042024 | TRIAL IMPLANT 5° H11mm |
03662663041928 | TRIAL IMPLANT 5° H09mm |
03662663041812 | TRIAL IMPLANT 0° H13mm |
03662663041751 | TRIAL IMPLANT 0° H11mm |
03662663041744 | TRIAL IMPLANT 0° H09mm |
03662663041737 | TRIAL IMPLANT 0° H07mm |
03662663041720 | IR923R |
03662663041713 | IR921R |
03662663041669 | IR919R |
03662663041652 | IR918R |
03662663041645 | IR917R |
03662663041638 | IR915R |
03662663041621 | IR914R |
03662663041348 | IR907R |
03662663041331 | IR906R |
03662663041225 | IR905R |
03662663041171 | IR904R |
03662663040716 | IR903R |
03662663040686 | IR902R |
03662663040587 | IR901R |
03662663040228 | IR900R |
03662663016049 | ROI V.B.R.8° L24 H13 |
03662663016032 | ROI V.B.R.8° L24 H11 |
03662663016025 | ROI V.B.R.8° L24 H09 |
03662663016018 | ROI V.B.R.5° L24 H13 |
03662663016001 | ROI V.B.R.5° L24 H11 |
03662663015998 | ROI V.B.R.5° L24 H09 |
03662663015981 | ROI V.B.R.0° L24 H11 |
03662663015974 | ROI V.B.R.0° L24 H09 |
03662663015967 | ROI VBR. 0° L24 H07 |
03662663015943 | ROI POSTERIOR CAGE 8° L24mm H13mm |