| Primary Device ID | 00853714008059 |
| NIH Device Record Key | cc808cdd-5a53-404a-98af-1965b58e43b5 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | LASS |
| Version Model Number | LP1001 |
| Catalog Number | LP1001 |
| Company DUNS | 079668796 |
| Company Name | RADUX DEVICES, LLC |
| 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 | true |
| Serial Number | false |
| Manufacturing Date | true |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Phone | 800-935-3137 |
| customerservice@raduxdevices.com | |
| Phone | 800-935-3137 |
| customerservice@raduxdevices.com | |
| Phone | 800-935-3137 |
| customerservice@raduxdevices.com | |
| Phone | 800-935-3137 |
| customerservice@raduxdevices.com | |
| Phone | 800-935-3137 |
| customerservice@raduxdevices.com | |
| Phone | 800-935-3137 |
| customerservice@raduxdevices.com | |
| Phone | 800-935-3137 |
| customerservice@raduxdevices.com | |
| Phone | 800-935-3137 |
| customerservice@raduxdevices.com | |
| Phone | 800-935-3137 |
| customerservice@raduxdevices.com | |
| Phone | 800-935-3137 |
| customerservice@raduxdevices.com | |
| Phone | 800-935-3137 |
| customerservice@raduxdevices.com | |
| Phone | 800-935-3137 |
| customerservice@raduxdevices.com | |
| Phone | 800-935-3137 |
| customerservice@raduxdevices.com | |
| Phone | 800-935-3137 |
| customerservice@raduxdevices.com | |
| Phone | 800-935-3137 |
| customerservice@raduxdevices.com | |
| Phone | 800-935-3137 |
| customerservice@raduxdevices.com | |
| Phone | 800-935-3137 |
| customerservice@raduxdevices.com | |
| Phone | 800-935-3137 |
| customerservice@raduxdevices.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00853714008059 [Primary] |
| CCX | Support, Patient Position |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-02-08 |
| Device Publish Date | 2024-01-31 |
| 00853714008073 | LASS Small Foam |
| 00853714008066 | LASS Large Foam |
| 00853714008059 | LASS Base Board |
| 00853714008042 | LASS Arm Board |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() LASS 88096064 not registered Dead/Abandoned |
Brain Contents Inc 2018-08-28 |
![]() LASS 79146500 4762352 Live/Registered |
LOCKDOWN MEDICAL LIMITED 2013-12-13 |
![]() LASS 78928085 not registered Dead/Abandoned |
BP Products North America Inc. 2006-07-12 |
![]() LASS 77935613 3849947 Live/Registered |
Lincoln Appraisal & Settlement Services, LLC 2010-02-15 |
![]() LASS 74619705 not registered Dead/Abandoned |
ASHLINE, CLIFFORD E. 1995-01-10 |
![]() LASS 74619705 not registered Dead/Abandoned |
ASHLINE, JUNE T. 1995-01-10 |
![]() LASS 74474510 1972143 Live/Registered |
TCOM, L.P. 1993-12-29 |
![]() LASS 74206301 1845337 Dead/Cancelled |
Messerschmitt-Bolkow-Blohm GmbH 1991-09-23 |
![]() LASS 74033942 1650551 Live/Registered |
LASS, INC. 1990-03-02 |