Ardis®
GUDID 00889024333734
ZIMMER SPINE, INC.
Metallic spinal interbody fusion cage| Primary Device ID | 00889024333734 |
| NIH Device Record Key | 738d6ec2-087c-41bc-9bb9-174b6ff9a522 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Ardis® |
| Version Model Number | 3201-110926 |
| 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 |
Customer Support Contacts
Device Dimensions
| Length | 26 Millimeter |
| Width | 9 Millimeter |
| Height | 11 Millimeter |
| Length | 26 Millimeter |
| Width | 9 Millimeter |
| Height | 11 Millimeter |
| Length | 26 Millimeter |
| Width | 9 Millimeter |
| Height | 11 Millimeter |
| Length | 26 Millimeter |
| Width | 9 Millimeter |
| Height | 11 Millimeter |
| Length | 26 Millimeter |
| Width | 9 Millimeter |
| Height | 11 Millimeter |
| Length | 26 Millimeter |
| Width | 9 Millimeter |
| Height | 11 Millimeter |
| Length | 26 Millimeter |
| Width | 9 Millimeter |
| Height | 11 Millimeter |
| Length | 26 Millimeter |
| Width | 9 Millimeter |
| Height | 11 Millimeter |
| Length | 26 Millimeter |
| Width | 9 Millimeter |
| Height | 11 Millimeter |
| Length | 26 Millimeter |
| Width | 9 Millimeter |
| Height | 11 Millimeter |
| Length | 26 Millimeter |
| Width | 9 Millimeter |
| Height | 11 Millimeter |
| Length | 26 Millimeter |
| Width | 9 Millimeter |
| Height | 11 Millimeter |
| Length | 26 Millimeter |
| Width | 9 Millimeter |
| Height | 11 Millimeter |
| Length | 26 Millimeter |
| Width | 9 Millimeter |
| Height | 11 Millimeter |
| Length | 26 Millimeter |
| Width | 9 Millimeter |
| Height | 11 Millimeter |
| Length | 26 Millimeter |
| Width | 9 Millimeter |
| Height | 11 Millimeter |
| Length | 26 Millimeter |
| Width | 9 Millimeter |
| Height | 11 Millimeter |
| Length | 26 Millimeter |
| Width | 9 Millimeter |
| Height | 11 Millimeter |
| Length | 26 Millimeter |
| Width | 9 Millimeter |
| Height | 11 Millimeter |
| Length | 26 Millimeter |
| Width | 9 Millimeter |
| Height | 11 Millimeter |
| Length | 26 Millimeter |
| Width | 9 Millimeter |
| Height | 11 Millimeter |
| Length | 26 Millimeter |
| Width | 9 Millimeter |
| Height | 11 Millimeter |
| Length | 26 Millimeter |
| Width | 9 Millimeter |
| Height | 11 Millimeter |
| Length | 26 Millimeter |
| Width | 9 Millimeter |
| Height | 11 Millimeter |
| Length | 26 Millimeter |
| Width | 9 Millimeter |
| Height | 11 Millimeter |
| Length | 26 Millimeter |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00889024333734 [Primary] |
FDA Product Code
| MAX | Intervertebral fusion device with bone graft, lumbar |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2020-02-24 |
| Device Publish Date | 2015-10-20 |
On-Brand Devices [Ardis®]
Trademark Results [Ardis]
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 |
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.