| Primary Device ID | 00887868269370 |
| NIH Device Record Key | cb4af6fe-9d16-4e1c-9cda-0ae66260aeda |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Ventix™ |
| Version Model Number | 110025990 |
| Catalog Number | 110025990 |
| 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 | 00887868269370 [Primary] |
| HIBCC | M5431100259901 [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 |