Primary Device ID | 20858293006421 |
NIH Device Record Key | 1f16b63f-8bfc-419f-bf6f-5cdfc5df3fcf |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Accu-Read |
Version Model Number | BP00-1101 |
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 | 00858293006427 [Primary] |
GS1 | 10858293006424 [Package] Contains: 00858293006427 Package: Bag [5 Units] In Commercial Distribution |
GS1 | 20858293006421 [Package] Contains: 00858293006427 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 |
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 |