| 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 |