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 |