Primary Device ID | 00860003643136 |
NIH Device Record Key | ae02cc23-1f09-4ddd-a795-b3265f192c33 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ResQUp |
Version Model Number | Sea Salt |
Company DUNS | 017840548 |
Company Name | Safe Patient Solutions, L.L.C. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
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 | false |
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 | true |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00860003643136 [Primary] |
IKX | Aid, Transfer |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-03-17 |
Device Publish Date | 2022-03-09 |
00860003643129 | Self-Recovery device to assist a fallen person moving themselves to a seated position after a no |
00860003643112 | Self-Recovery device to assist a fallen person moving themselves to a seated position after a no |
00860003643105 | Self-Recovery device to assist a fallen person moving themselves to a seated position after a no |
00860003643136 | Self-Recovery device to assist a fallen person moving themselves to a seated position after a no |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
RESQUP 88265528 not registered Live/Pending |
Safe Patient Solutions, L.L.C. 2019-01-17 |