| Primary Device ID | 20653405014574 |
| NIH Device Record Key | 0e7f3639-baf5-45e7-8ca5-05e0191f8743 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | VENI-GARD |
| Version Model Number | 740-1440 |
| Catalog Number | 740-1440 |
| Company DUNS | 071595540 |
| Company Name | Conmed Corporation |
| Device Count | 500 |
| 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 | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Storage Environment Humidity | Between 10 Degrees Celsius and 32 Degrees Celsius |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00653405014570 [Unit of Use] |
| GS1 | 10653405014577 [Primary] |
| GS1 | 20653405014574 [Package] Contains: 10653405014577 Package: Box [500 Units] In Commercial Distribution |
| MGP | Dressing, wound and burn, occlusive |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-05-06 |
| Device Publish Date | 2020-04-28 |
| 20653405014642 | VeniGard ML |
| 20653405014611 | Veni-Gard TPN |
| 20653405014574 | Veni-Gard AP |
| 20653405014437 | 730-4432B Veni-Gard TM Jr. Bulk |
| 20653405014420 | Veni-Gard TM Jr. |
| 20653405014338 | Veni-Gard SP Bulk |
| 20653405014321 | Veni-Gard SP |
| 20653405014277 | 705-4431B VeniGard TM Bulk |
| 20653405014260 | VeniGard TM |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() VENI-GARD 73250073 1201734 Live/Registered |
Consolidated Medical Equipment Inc. 1980-02-13 |