Primary Device ID | 00889024109445 |
NIH Device Record Key | 389ad629-c670-4df5-bcfe-239d579db602 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | V-TEK™ |
Version Model Number | 28.25.410 |
Company DUNS | 488133448 |
Company Name | Zimmer GmbH |
Device Count | 1 |
DM Exempt | true |
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 |
Phone | +1(800)348-2759 |
zimmer.consumerrelations@zimmer.com | |
Phone | +1(800)348-2759 |
zimmer.consumerrelations@zimmer.com |
Outer Diameter | 2.7 Millimeter |
Length | 10 Millimeter |
Device Size Text, specify | 0 |
Outer Diameter | 2.7 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00889024109445 [Primary] |
HWC | Screw, fixation, bone |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00889024109445]
Moist Heat or Steam Sterilization
[00889024109445]
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 | 2016-12-30 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
V-TEK 78521970 not registered Dead/Abandoned |
Kalil, Anthony 2004-11-23 |
V-TEK 76437480 2719250 Dead/Cancelled |
SUPERIOR TATTOO EQUIPMENT, INC. 2002-08-05 |
V-TEK 74412774 1872299 Live/Registered |
V-TEK, INC. 1993-07-15 |