| Primary Device ID | 20858293006414 |
| NIH Device Record Key | 400737d4-d2b9-4e62-a9a1-78cad9254db7 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Accu-Read |
| Version Model Number | BP00-0101 |
| Company DUNS | 796083392 |
| Company Name | REPROCESSING PRODUCTS CORPORATION |
| 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 | false |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00858293006410 [Primary] |
| GS1 | 10858293006417 [Package] Contains: 00858293006410 Package: Bag [5 Units] In Commercial Distribution |
| GS1 | 20858293006414 [Package] Contains: 00858293006410 Package: Bag [20 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 | 2019-09-06 |
| Device Publish Date | 2019-08-29 |
| 10858293006448 | BP Cuff, Adult Thigh, 1 Tube BP00-3105 = 5 pack |
| 20858293006438 | BP Cuff, Adult Large, 1 Tube BP00-2105 = 5 pack BP00-2120 = 20 pack |
| 20858293006421 | BP Cuff, Adult Regular, 1 tube BP00-1105 = 5 pack BP00-1120 = 20 pack |
| 20858293006414 | BP Cuff, Adult Sm, 1 tube BP00-0105 = 5 pack BP00-0120 = 20 pack |
| 00858293006915 | BP Cuff, Adult Lg, 2 tube BP00-2205 = 5 pack |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() ACCU-READ 78564329 3679809 Dead/Cancelled |
Reprocessing Products Corporation (RPC) 2005-02-10 |
![]() ACCU-READ 74467828 1924496 Dead/Cancelled |
SUNBEAM CORPORATION 1993-12-09 |