Primary Device ID | 00860002071237 |
NIH Device Record Key | 1440dde4-d1f2-4bec-ba12-53dbc6ceb5a5 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Ease Cushion |
Version Model Number | Lite |
Company DUNS | 080264585 |
Company Name | Ease Seating Systems |
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 | true |
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 | 00860002071237 [Primary] |
FNM | Mattress, Air Flotation, Alternating Pressure |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2021-02-19 |
Device Publish Date | 2020-11-09 |
00860002071213 | Overlay |
00860002071206 | 20" x 20" cushion |
00860000915397 | 20" x 18" cushion |
00860000915380 | 20" x 16" cushion |
00860000915373 | 18" x 20" cushion |
00860000915366 | 18" x 18" cushion |
00860000915359 | 18" x 16" cushion |
00860000915342 | 16" x 20" |
00860000915335 | 16" x 18" cushion |
00860000915328 | 16" x 16" cushion |
00860000915311 | Patient Matched Cushion |
00860000915304 | Ease Cushion Pump |
00860002071220 | Ease Cushion Standard Pump |
00860002071237 | Lite |
00860010877432 | Gen 1 22x22 |
00860010877425 | Gen 1 16x16 |
00860010877418 | Gen 1 18x18 |
00860010877401 | Gen 1 20x20 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() EASE CUSHION 88623507 not registered Live/Pending |
JRD Enterprises, LLC 2019-09-19 |