| Primary Device ID | 00889024318311 |
| NIH Device Record Key | 72c47646-c217-47a1-b215-315cbdc95b4d |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Mergence™-S |
| Version Model Number | 96-108-67051 |
| 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 | false |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| 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 |
| Height | 5 Millimeter |
| Device Size Text, specify | 0 |
| Height | 5 Millimeter |
| Device Size Text, specify | 0 |
| Height | 5 Millimeter |
| Device Size Text, specify | 0 |
| Height | 5 Millimeter |
| Device Size Text, specify | 0 |
| Height | 5 Millimeter |
| Device Size Text, specify | 0 |
| Height | 5 Millimeter |
| Device Size Text, specify | 0 |
| Height | 5 Millimeter |
| Device Size Text, specify | 0 |
| Height | 5 Millimeter |
| Device Size Text, specify | 0 |
| Height | 5 Millimeter |
| Device Size Text, specify | 0 |
| Height | 5 Millimeter |
| Device Size Text, specify | 0 |
| Height | 5 Millimeter |
| Device Size Text, specify | 0 |
| Height | 5 Millimeter |
| Device Size Text, specify | 0 |
| Height | 5 Millimeter |
| Device Size Text, specify | 0 |
| Height | 5 Millimeter |
| Device Size Text, specify | 0 |
| Height | 5 Millimeter |
| Device Size Text, specify | 0 |
| Height | 5 Millimeter |
| Device Size Text, specify | 0 |
| Height | 5 Millimeter |
| Device Size Text, specify | 0 |
| Height | 5 Millimeter |
| Device Size Text, specify | 0 |
| Height | 5 Millimeter |
| Device Size Text, specify | 0 |
| Height | 5 Millimeter |
| Device Size Text, specify | 0 |
| Height | 5 Millimeter |
| Device Size Text, specify | 0 |
| Height | 5 Millimeter |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00889024318311 [Primary] |
| ODP | Intervertebral fusion device with bone graft, cervical |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00889024318311]
Moist Heat or Steam Sterilization
[00889024318311]
Moist Heat or Steam Sterilization
[00889024318311]
Moist Heat or Steam Sterilization
[00889024318311]
Moist Heat or Steam Sterilization
[00889024318311]
Moist Heat or Steam Sterilization
[00889024318311]
Moist Heat or Steam Sterilization
[00889024318311]
Moist Heat or Steam Sterilization
[00889024318311]
Moist Heat or Steam Sterilization
[00889024318311]
Moist Heat or Steam Sterilization
[00889024318311]
Moist Heat or Steam Sterilization
[00889024318311]
Moist Heat or Steam Sterilization
[00889024318311]
Moist Heat or Steam Sterilization
[00889024318311]
Moist Heat or Steam Sterilization
[00889024318311]
Moist Heat or Steam Sterilization
[00889024318311]
Moist Heat or Steam Sterilization
[00889024318311]
Moist Heat or Steam Sterilization
[00889024318311]
Moist Heat or Steam Sterilization
[00889024318311]
Moist Heat or Steam Sterilization
[00889024318311]
Moist Heat or Steam Sterilization
[00889024318311]
Moist Heat or Steam Sterilization
[00889024318311]
Moist Heat or Steam Sterilization
[00889024318311]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2017-09-20 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() MERGENCE 77052371 3606453 Live/Registered |
Zimmer Biomet Spine, Inc. 2006-11-28 |