Universal Clamp ™
GUDID 00889024342651
ZIMMER SPINE
Metallic spinal interbody fusion cage| Primary Device ID | 00889024342651 |
| NIH Device Record Key | 029831db-fedb-4ea0-99a0-57f7017794c5 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Universal Clamp ™ |
| Version Model Number | SNA027-0-20055 |
| 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 | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
Customer Support Contacts
Device Dimensions
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00889024342651 [Primary] |
FDA Product Code
| OWI | Bone fixation cerclage, sublaminar |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2020-02-24 |
| Device Publish Date | 2015-10-20 |
On-Brand Devices [Universal Clamp ™]
| 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 |
Trademark Results [Universal Clamp]
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 |
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.