| Primary Device ID | 00889024637962 |
| NIH Device Record Key | bea97618-5f16-4be0-88de-8d0099067757 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Trilogy® |
| Version Model Number | 6120-72-32 |
| Catalog Number | 00-6120-072-32 |
| Company DUNS | 056038268 |
| Company Name | Zimmer, 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 Size Text, specify | 0 |
| Lumen/Inner Diameter | 32 Millimeter |
| Device Size Text, specify | 0 |
| Lumen/Inner Diameter | 32 Millimeter |
| Device Size Text, specify | 0 |
| Lumen/Inner Diameter | 32 Millimeter |
| Device Size Text, specify | 0 |
| Lumen/Inner Diameter | 32 Millimeter |
| Device Size Text, specify | 0 |
| Lumen/Inner Diameter | 32 Millimeter |
| Device Size Text, specify | 0 |
| Lumen/Inner Diameter | 32 Millimeter |
| Device Size Text, specify | 0 |
| Lumen/Inner Diameter | 32 Millimeter |
| Device Size Text, specify | 0 |
| Lumen/Inner Diameter | 32 Millimeter |
| Device Size Text, specify | 0 |
| Lumen/Inner Diameter | 32 Millimeter |
| Device Size Text, specify | 0 |
| Lumen/Inner Diameter | 32 Millimeter |
| Device Size Text, specify | 0 |
| Lumen/Inner Diameter | 32 Millimeter |
| Device Size Text, specify | 0 |
| Lumen/Inner Diameter | 32 Millimeter |
| Device Size Text, specify | 0 |
| Lumen/Inner Diameter | 32 Millimeter |
| Device Size Text, specify | 0 |
| Lumen/Inner Diameter | 32 Millimeter |
| Device Size Text, specify | 0 |
| Lumen/Inner Diameter | 32 Millimeter |
| Device Size Text, specify | 0 |
| Lumen/Inner Diameter | 32 Millimeter |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00889024637962 [Primary] |
| MLR | Sterilizer, chemical |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2022-03-07 |
| Device Publish Date | 2022-02-25 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() TRILOGY 97927068 not registered Live/Pending |
Trilogy Solutions, LLC 2023-05-09 |
![]() TRILOGY 97904591 not registered Live/Pending |
Brett-Young Seeds Ltd. 2023-04-24 |
![]() TRILOGY 97457869 not registered Live/Pending |
The Shepherd Institute 2022-06-14 |
![]() TRILOGY 97240248 not registered Live/Pending |
Trilogy Enterprises, Inc. 2022-01-26 |
![]() TRILOGY 90885268 not registered Live/Pending |
FAIRMONT HOLDINGS, INC. 2021-08-16 |
![]() TRILOGY 90876909 not registered Live/Pending |
Trilogy 5G, Inc. 2021-08-11 |
![]() TRILOGY 90876907 not registered Live/Pending |
Trilogy 5G, Inc. 2021-08-11 |
![]() TRILOGY 90843842 not registered Live/Pending |
Trilogy Health Services, LLC 2021-07-22 |
![]() TRILOGY 90518681 not registered Live/Pending |
E. P. Henry Corporation 2021-02-08 |
![]() TRILOGY 90455868 not registered Live/Pending |
Secada Medical LLC 2021-01-08 |
![]() TRILOGY 90334762 not registered Live/Pending |
KAZAG 2020-11-21 |
![]() TRILOGY 90196375 not registered Live/Pending |
Everi Payments Inc. 2020-09-21 |