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 |