Primary Device ID | 00841439111918 |
NIH Device Record Key | 2500e59e-6c11-4e57-8598-4bb7b9d9d2c3 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Feetfix™ MR Platform |
Version Model Number | 302071MR |
Catalog Number | 302071MR |
Company DUNS | 103977526 |
Company Name | MEDTEC, INC. |
Device Count | 1 |
DM Exempt | true |
Pre-market Exempt | false |
MRI Safety Status | MR Conditional |
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 | 00841439111918 [Primary] |
LNH | System, nuclear magnetic resonance imaging |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2019-05-31 |
Device Publish Date | 2018-08-20 |
00841439114650 - Pronumbra | 2025-09-22 Pronumbra Helping Hand, Left |
00841439114674 - Pronumbra | 2025-09-22 Pronumbra Helping Hand, Right |
00841439114681 - Pronumbra | 2025-09-22 Pronumbra 130cm kVue |
00841439114698 - Pronumbra | 2025-09-22 Pronumbra Neck Support, 40mm |
00841439114704 - Pronumbra | 2025-09-22 Pronumbra Neck Support, 50mm |
00841439114711 - Pronumbra | 2025-09-22 Pronumbra Neck Support, 65mm |
00841439114728 - Pronumbra | 2025-09-22 Pronumbra Shoulder Adapter |
00841439114841 - ZiFix Traverse | 2025-09-22 ZiFix Traverse with ONEClamp |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() FEETFIX 98185639 not registered Live/Pending |
Fix Digital Incorporated 2023-09-18 |