Primary Device ID | 00841439109953 |
NIH Device Record Key | 04158506-929c-4ec1-8722-170081c08650 |
Commercial Distribution Discontinuation | 2020-01-20 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | Combifix™ |
Version Model Number | 151005 |
Catalog Number | 151005 |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00841439109953 [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 | 7 |
Public Version Date | 2020-01-20 |
Device Publish Date | 2017-08-02 |
00841439111901 | baseplate with (2) elevation blocks, Feetfix™ bracket, Feetfix™ cushion, and Kneefix™ cush |
00841439111895 | baseplate with (2) elevation blocks, Feetfix™ bracket, Feetfix™ cushion, and Kneefix™ cush |
00841439109953 | Reusable non-sterile Combifix™ baseplate with (2) elevation blocks, Feetfix™ bracket, Feetfi |
00841439109946 | baseplate with (2) elevation blocks, Feetfix™ bracket, Feetfix™ cushion, and Kneefix™ cush |
00841439100813 | Reusable non-sterile Combifix™ baseplate with (2) elevation blocks, Feetfix™ bracket, Feetfi |
00841439100806 | baseplate with (2) elevation blocks, Feetfix™ bracket, Feetfix™ cushion, and Kneefix™ cush |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() COMBIFIX 74269878 not registered Dead/Abandoned |
E. R. Squibb & Sons, Inc. 1992-04-27 |
![]() COMBIFIX 72282148 0868948 Dead/Expired |
TESA S.A. 1967-10-09 |