| Primary Device ID | 20889483631611 |
| NIH Device Record Key | e7dd4949-2307-4cd3-a4cf-0a00492fb704 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | DuraCheck |
| Version Model Number | ZDC4301HP-10 |
| Company DUNS | 022721133 |
| Company Name | SALTER LABS |
| 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 | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 10889483631614 [Primary] |
| GS1 | 20889483631611 [Package] Contains: 10889483631614 Package: Box [10 Units] In Commercial Distribution |
| GS1 | 30889483631618 [Package] Package: Case [100 Units] In Commercial Distribution |
| DXQ | Blood Pressure Cuff |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-12-09 |
| Device Publish Date | 2024-11-29 |
| 20889483631666 | DuraCheck Reusable Blood Pressure Cuff Thigh |
| 20889483631659 | DuraCheck Reusable Blood Pressure Cuff Large Adult Long |
| 20889483631642 | DuraCheck Reusable Blood Pressure Cuff Large Adult |
| 20889483631635 | DuraCheck Reusable Blood Pressure Cuff Adult Long |
| 20889483631628 | DuraCheck Reusable Blood Pressure Cuff Adult |
| 20889483631611 | DuraCheck Reusable Blood Pressure Cuff Small Adult |
| 20889483631604 | DuraCheck Reusable Blood Pressure Cuff Child |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() DURACHECK 73763141 1554371 Dead/Cancelled |
MONSANTO COMPANY 1988-11-14 |