Primary Device ID | 03662663002127 |
NIH Device Record Key | 4df5fd06-5233-477f-a0d7-21c9fab50019 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Easyspine |
Version Model Number | ES016T |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 03662663002127 [Primary] |
NKB | Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease |
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 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
EASYSPINE 78941231 not registered Dead/Abandoned |
ACCO Brands Corporation 2006-07-31 |
EASYSPINE 78514775 3155009 Live/Registered |
LDR MEDICAL, S.A.S. 2004-11-10 |
EASYSPINE 77467257 3566916 Live/Registered |
ACCO Brands Corporation 2008-05-06 |