Primary Device ID | 00846795014439 |
NIH Device Record Key | a126ebda-4cc6-4c9a-9b75-c7df0e58a759 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Stablecut® Vanguard™ |
Version Model Number | 32700367 |
Company DUNS | 137354267 |
Company Name | ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS, 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 | 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 | 00846795014439 [Primary] |
GFA | BLADE, SAW, GENERAL & PLASTIC SURGERY, SURGICAL |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2019-07-12 |
Device Publish Date | 2017-04-28 |
00846795027408 | 32700389 |
00846795027392 | 32700368 |
00846795014446 | 32700369 |
00846795014439 | 32700367 |
00889024497405 | 32700389 |
00889024497368 | 32700369 |
00889024497351 | 32700368 |
00889024497344 | 32700367 |
00889024647640 | 32700369 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
STABLECUT 85211274 3990180 Live/Registered |
Synvasive Technology, Inc. 2011-01-05 |
STABLECUT 76393707 2672143 Dead/Cancelled |
SYNVASIVE TECHNOLOGY, INC. 2002-04-09 |
STABLECUT 74299253 1758178 Dead/Cancelled |
Sierra Surgical, Inc. 1992-07-28 |