| Primary Device ID | 00841439106877 |
| NIH Device Record Key | cffdc2af-9547-43ab-9486-9b263023969e |
| Commercial Distribution Discontinuation | 2019-05-20 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | Alignment Block |
| Version Model Number | MTNW425200 |
| Catalog Number | MTNW425200 |
| Company DUNS | 103977526 |
| Company Name | MEDTEC, INC. |
| Device Count | 1 |
| DM Exempt | true |
| Pre-market Exempt | true |
| 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 | false |
| 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 |
| Length | 10 Centimeter |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00841439106877 [Primary] |
| IXG | Phantom, anthropomorphic, radiographic |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2019-05-20 |
| Device Publish Date | 2017-08-02 |
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