| Primary Device ID | 00889024315808 |
| NIH Device Record Key | fd22eff8-627b-4e7f-8f71-8fbde206b93b |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | TM Ardis® Trabecular Metal™ |
| Version Model Number | 06-701-02141 |
| Company DUNS | 793120965 |
| Company Name | ZIMMER TRABECULAR METAL TECHNOLOGY 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 | +1(800)348-2759 |
| zimmer.consumerrelations@zimmer.com | |
| Phone | +1(800)348-2759 |
| zimmer.consumerrelations@zimmerbiomet.com |
| Length | 26 Millimeter |
| Height | 14 Millimeter |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00889024315808 [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 | 4 |
| Public Version Date | 2020-02-24 |
| Device Publish Date | 2015-09-17 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() TM ARDIS 85541803 4354906 Live/Registered |
Zimmer Biomet Spine, Inc. 2012-02-14 |