Primary Device ID | 00889024489417 |
NIH Device Record Key | c93d2d67-6213-45cb-92a3-9e935d604c83 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Universal Clamp ™ |
Version Model Number | SN2027-0-00006 |
Catalog Number | SN2027-0-00006 |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00889024489417 [Primary] |
JDQ | Cerclage, Fixation |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2017-05-24 |
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 |