| Primary Device ID | 00889024685475 |
| NIH Device Record Key | 70bb2ce5-5615-497d-8d5f-26ae2a99731d |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Comprehensive Reverse |
| Version Model Number | 120001781 |
| Catalog Number | 120001781 |
| Company DUNS | 056038268 |
| Company Name | Zimmer, Inc. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| Expiration Date | false |
| 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@zimmerbiomet.com | |
| Phone | +1(800)348-2759 |
| zimmer.consumerrelations@zimmerbiomet.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00889024685475 [Primary] |
| FSM | TRAY, SURGICAL, INSTRUMENT |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00889024685475]
Moist Heat or Steam Sterilization
[00889024685475]
Moist Heat or Steam Sterilization
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2025-09-15 |
| Device Publish Date | 2025-09-05 |
| 00889024685383 - Comprehensive Humeral | 2025-09-15 |
| 00889024685413 - Comprehensive Humeral | 2025-09-15 |
| 00889024685420 - Comprehensive Humeral | 2025-09-15 |
| 00889024685437 - Alliance Glenoid, Identity Humeral | 2025-09-15 |
| 00889024685444 - Comprehensive Humeral | 2025-09-15 |
| 00889024685475 - Comprehensive Reverse | 2025-09-15 |
| 00889024685475 - Comprehensive Reverse | 2025-09-15 |
| 00889024685499 - Comprehensive Humeral | 2025-09-15 |
| 00889024685512 - Comprehensive Humeral | 2025-09-15 |