| Primary Device ID | 00889024342644 |
| NIH Device Record Key | 43972d23-aecb-47c6-9ffa-c70761192710 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Universal Clamp ™ |
| Version Model Number | SNA027-0-20000 |
| Company DUNS | 391738585 |
| Company Name | ZIMMER SPINE |
| 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 | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00889024342644 [Primary] |
| OWI | Bone fixation cerclage, sublaminar |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2020-02-24 |
| Device Publish Date | 2015-10-02 |
| 00889024342699 | SNA027-0-30063 |
| 00889024342682 | SNA027-0-30060 |
| 00889024342675 | SNA027-0-30055 |
| 00889024342668 | SNA027-0-20060 |
| 00889024342651 | SNA027-0-20055 |
| 00889024342644 | SNA027-0-20000 |
| 00889024489424 | SNA027-0-30006S |
| 00889024489417 | SN2027-0-00006 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() UNIVERSAL CLAMP 98691224 not registered Live/Pending |
KOSMEK LTD. 2024-08-09 |
![]() UNIVERSAL CLAMP 86136992 4604593 Live/Registered |
Zimmer Spine SAS 2013-12-06 |
![]() UNIVERSAL CLAMP 78860100 3364015 Dead/Cancelled |
Zimmer Spine SAS 2006-04-12 |