Primary Device ID | 00889024110205 |
NIH Device Record Key | 1dce5083-a39f-483b-9a46-4a9bfcc0255f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | V-TEK™ |
Version Model Number | 28.65.034 |
Company DUNS | 488133448 |
Company Name | Zimmer GmbH |
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 |
Phone | +1(800)348-2759 |
zimmer.consumerrelations@zimmer.com | |
Phone | +1(800)348-2759 |
zimmer.consumerrelations@zimmer.com |
Outer Diameter | 3 Millimeter |
Device Size Text, specify | 0 |
Length | 34 Millimeter |
Outer Diameter | 3 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00889024110205 [Primary] |
HTN | WASHER, BOLT NUT |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00889024110205]
Moist Heat or Steam Sterilization
[00889024110205]
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 |