| Primary Device ID | 00813830023572 |
| NIH Device Record Key | 6be960fa-2bb0-4d1d-820c-dfa774646ab8 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Accu-Vac |
| Version Model Number | 56955 |
| Catalog Number | 56955 |
| Company DUNS | 088302096 |
| Company Name | ACCUTRON, INC. |
| 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 | false |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00813830023572 [Primary] |
| CBN | Apparatus, Gas-Scavenging |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-09-28 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() ACCU-VAC 75804230 2371194 Live/Registered |
Morris Bean & Company 1999-09-21 |
![]() ACCU-VAC 74613665 2022468 Dead/Cancelled |
KADANT INC. 1994-12-21 |
![]() ACCU-VAC 73564644 1426341 Dead/Cancelled |
FLO-BOB INDUSTRIES INCORPORATED 1985-10-23 |