Primary Device ID | 00841439111574 |
NIH Device Record Key | 6044521b-bcfc-4d9a-9f66-51bd0e02bdf9 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Immobilizer |
Version Model Number | MTDLIZ2 |
Catalog Number | MTDLIZ2 |
Company DUNS | 103977526 |
Company Name | MEDTEC, INC. |
Device Count | 1 |
DM Exempt | true |
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 | 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 | +1(712)737-8688 |
radiotherapy.complaints@civcort.com |
Width | 18.3 Inch |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00841439111574 [Primary] |
IYE | Accelerator, linear, medical |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 5 |
Public Version Date | 2020-03-19 |
Device Publish Date | 2018-03-01 |
00841439111574 | dual low leg |
00841439111567 | dual leg |
00841439104187 | Reusable non-sterile (84 x 46 x 28cm) dual leg immobilizer |
00841439104170 | Reusable non-sterile (84 x 46 x 28cm) dual leg immobilizer |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() IMMOBILIZER 80983660 0983660 Dead/Cancelled |
Astrum Research & Chemical Corporation 0000-00-00 |
![]() IMMOBILIZER 76298894 not registered Dead/Abandoned |
Exiqon A/S 2001-08-14 |
![]() IMMOBILIZER 76074274 2703285 Dead/Cancelled |
TELEFLEX MEDICAL INCORPORATED 2000-06-20 |
![]() IMMOBILIZER 74552249 not registered Dead/Abandoned |
Bianco, Thomas A., Sr. 1994-07-22 |
![]() IMMOBILIZER 73332471 1214824 Dead/Cancelled |
H & H Plastic Mfg. Co. 1981-10-15 |