Primary Device ID | 03662663025034 |
NIH Device Record Key | c5447158-ebc8-4cb8-8152-e7bf1caa6b70 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | VFT |
Version Model Number | VF1313P |
Catalog Number | VF1313P |
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 | 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 |
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 | |
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 |
Height | 44 Millimeter |
Height | 44 Millimeter |
Height | 44 Millimeter |
Height | 44 Millimeter |
Height | 44 Millimeter |
Height | 44 Millimeter |
Height | 44 Millimeter |
Height | 44 Millimeter |
Height | 44 Millimeter |
Height | 44 Millimeter |
Height | 44 Millimeter |
Height | 44 Millimeter |
Height | 44 Millimeter |
Height | 44 Millimeter |
Height | 44 Millimeter |
Height | 44 Millimeter |
Height | 44 Millimeter |
Height | 44 Millimeter |
Height | 44 Millimeter |
Height | 44 Millimeter |
Height | 44 Millimeter |
Height | 44 Millimeter |
Height | 44 Millimeter |
Height | 44 Millimeter |
Height | 44 Millimeter |
Height | 44 Millimeter |
Height | 44 Millimeter |
Height | 44 Millimeter |
Height | 44 Millimeter |
Height | 44 Millimeter |
Height | 44 Millimeter |
Height | 44 Millimeter |
Height | 44 Millimeter |
Height | 44 Millimeter |
Height | 44 Millimeter |
Height | 44 Millimeter |
Height | 44 Millimeter |
Height | 44 Millimeter |
Height | 44 Millimeter |
Height | 44 Millimeter |
Height | 44 Millimeter |
Height | 44 Millimeter |
Height | 44 Millimeter |
Height | 44 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 03662663025034 [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 | 4 |
Public Version Date | 2020-02-24 |
Device Publish Date | 2017-05-19 |