Primary Device ID | 00841439114643 |
NIH Device Record Key | c4fe4572-0ace-4400-920a-a728da749c52 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Wedge and Spacer Set |
Version Model Number | 107106MR |
Catalog Number | 107106MR |
Company DUNS | 103977526 |
Company Name | MEDTEC, INC. |
Device Count | 1 |
DM Exempt | true |
Pre-market Exempt | false |
MRI Safety Status | MR Safe |
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 | |
Phone | +1(712)737-8688 |
radiotherapy.complaints@civcort.com | |
Phone | +1(712)737-8688 |
radiotherapy.complaints@civcort.com | |
Phone | +1(712)737-8688 |
radiotherapy.complaints@civcort.com | |
Phone | +1(712)737-8688 |
radiotherapy.complaints@civcort.com | |
Phone | +1(712)737-8688 |
radiotherapy.complaints@civcort.com | |
Phone | +1(712)737-8688 |
radiotherapy.complaints@civcort.com | |
Phone | +1(712)737-8688 |
radiotherapy.complaints@civcort.com | |
Phone | +1(712)737-8688 |
radiotherapy.complaints@civcort.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00841439114643 [Primary] |
IYE | Accelerator, linear, medical |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-07-17 |
Device Publish Date | 2024-07-09 |
00841439111086 | 2.5 degree wedge, 5 degree wedge, 20mm spacer, and 30mm spacer |
00841439114643 | 2.5 degree wedge, 5 degree wedge, 20mm spacer, and 30mm spacer, MR |