Primary Device ID | 00887868269387 |
NIH Device Record Key | 8e96a08e-3565-4296-9254-3b6221fc6103 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Ventix™ |
Version Model Number | 110025992 |
Catalog Number | 110025992 |
Company DUNS | 606719685 |
Company Name | CAYENNE MEDICAL, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Safe |
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 | 00887868269387 [Primary] |
HIBCC | M5431100259921 [Previous] |
MBI | Fastener, Fixation, Nondegradable, Soft Tissue |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-09-29 |
Device Publish Date | 2020-09-21 |
00887868269387 | 110025992 |
00887868269370 | 110025990 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
VENTIX 88182771 not registered Live/Pending |
Biomet Manufacturing, LLC 2018-11-06 |
VENTIX 86626579 not registered Dead/Abandoned |
Biomet Sports Medicine, LLC 2015-05-12 |
VENTIX 75484798 not registered Dead/Abandoned |
LearningSTATE, Inc. 1998-05-14 |
VENTIX 75484797 not registered Dead/Abandoned |
VENTIX SYSTEMS, INC. 1998-05-14 |