Primary Device ID | 00889024333727 |
NIH Device Record Key | 458a5ba4-48eb-46c1-ac1e-57d2d9be1270 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Ardis® |
Version Model Number | 3201-110922 |
Company DUNS | 787663400 |
Company Name | ZIMMER SPINE, 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 |
Width | 9 Millimeter |
Length | 22 Millimeter |
Height | 11 Millimeter |
Width | 9 Millimeter |
Length | 22 Millimeter |
Height | 11 Millimeter |
Width | 9 Millimeter |
Length | 22 Millimeter |
Height | 11 Millimeter |
Width | 9 Millimeter |
Length | 22 Millimeter |
Height | 11 Millimeter |
Width | 9 Millimeter |
Length | 22 Millimeter |
Height | 11 Millimeter |
Width | 9 Millimeter |
Length | 22 Millimeter |
Height | 11 Millimeter |
Width | 9 Millimeter |
Length | 22 Millimeter |
Height | 11 Millimeter |
Width | 9 Millimeter |
Length | 22 Millimeter |
Height | 11 Millimeter |
Width | 9 Millimeter |
Length | 22 Millimeter |
Height | 11 Millimeter |
Width | 9 Millimeter |
Length | 22 Millimeter |
Height | 11 Millimeter |
Width | 9 Millimeter |
Length | 22 Millimeter |
Height | 11 Millimeter |
Width | 9 Millimeter |
Length | 22 Millimeter |
Height | 11 Millimeter |
Width | 9 Millimeter |
Length | 22 Millimeter |
Height | 11 Millimeter |
Width | 9 Millimeter |
Length | 22 Millimeter |
Height | 11 Millimeter |
Width | 9 Millimeter |
Length | 22 Millimeter |
Height | 11 Millimeter |
Width | 9 Millimeter |
Length | 22 Millimeter |
Height | 11 Millimeter |
Width | 9 Millimeter |
Length | 22 Millimeter |
Height | 11 Millimeter |
Width | 9 Millimeter |
Length | 22 Millimeter |
Height | 11 Millimeter |
Width | 9 Millimeter |
Length | 22 Millimeter |
Height | 11 Millimeter |
Width | 9 Millimeter |
Length | 22 Millimeter |
Height | 11 Millimeter |
Width | 9 Millimeter |
Length | 22 Millimeter |
Height | 11 Millimeter |
Width | 9 Millimeter |
Length | 22 Millimeter |
Height | 11 Millimeter |
Width | 9 Millimeter |
Length | 22 Millimeter |
Height | 11 Millimeter |
Width | 9 Millimeter |
Length | 22 Millimeter |
Height | 11 Millimeter |
Width | 9 Millimeter |
Length | 22 Millimeter |
Height | 11 Millimeter |
Width | 9 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00889024333727 [Primary] |
MAX | Intervertebral fusion device with bone graft, lumbar |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2020-02-24 |
Device Publish Date | 2015-10-20 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
ARDIS 97806326 not registered Live/Pending |
Ardis Dispute Resolution, P.B.C. 2023-02-22 |
ARDIS 97702088 not registered Live/Pending |
KBR Wyle Services, LLC 2022-12-02 |
ARDIS 90083919 not registered Live/Pending |
Ardis Welness, LLC 2020-07-30 |
ARDIS 88316384 not registered Live/Pending |
Ardis Wellness, LLC 2019-02-26 |
ARDIS 79272389 not registered Live/Pending |
ARDIS INFORMATION SYSTEMS NV 2019-09-16 |
ARDIS 79002655 3029285 Dead/Cancelled |
Eberhard-Karls-Universität Tübingen Universitätsklinikum 2003-12-22 |
ARDIS 77293169 3535083 Live/Registered |
ZIMMER BIOMET SPINE, INC. 2007-10-01 |
ARDIS 74048822 1653230 Dead/Cancelled |
ARDIS Company 1990-04-12 |
ARDIS 74048821 1651720 Dead/Cancelled |
ARDIS COMPANY 1990-04-12 |
ARDIS 74048820 1877124 Dead/Cancelled |
ARDIS Company 1990-04-12 |
ARDIS 74048819 1647678 Dead/Cancelled |
ARDIS Company 1990-04-12 |
ARDIS 74048818 1649711 Dead/Cancelled |
ARDIS COMPANY 1990-04-12 |