| Primary Device ID | 00812444027372 |
| NIH Device Record Key | 3a195ab5-f1f4-4ac3-b64c-3c5498ab7a6b |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Powertape |
| Version Model Number | TAPRPBB001 |
| Company DUNS | 964053560 |
| Company Name | RIVERPOINT MEDICAL, LLC |
| 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 | true |
| Expiration Date | true |
| 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 | 00812444027372 [Primary] |
| GAT | Suture, Nonabsorbable, Synthetic, Polyethylene |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-04-07 |
| Device Publish Date | 2020-03-30 |
| 00812444027389 | suture |
| 00812444027372 | suture |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() POWERTAPE 78648460 3138427 Dead/Cancelled |
Pearson, Ronald K. 2005-06-10 |
![]() POWERTAPE 78473416 not registered Dead/Abandoned |
ANDOVER HEALTHCARE, INC. 2004-08-25 |
![]() POWERTAPE 76712048 4303119 Live/Registered |
Andover Healthcare, Inc. 2012-07-27 |
![]() POWERTAPE 76049629 2539478 Live/Registered |
BUDNICK CONVERTING, INC. 2000-05-15 |