| Primary Device ID | 00841439105245 |
| NIH Device Record Key | 1f4b2b6b-e711-49eb-b583-3435e3f49f0e |
| Commercial Distribution Discontinuation | 2020-01-13 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | Lateral Stabilizer |
| Version Model Number | MTIL600311 |
| Catalog Number | MTIL600311 |
| 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 |
| Width | 9.4 Inch |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00841439105245 [Primary] |
| IXQ | Table, radiographic, stationary top |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 6 |
| Public Version Date | 2020-01-13 |
| Device Publish Date | 2017-08-02 |
| 00841439105849 | For use with GE VCT Global 2000 CT |
| 00841439105818 | For use with GE VCT Global 1700 CT |
| 00841439105788 | Reusable non-sterile lateral stabilizer for use with GE Discovery ST CT |
| 00841439105740 | For use with GE Hi-Speed CT |
| 00841439105245 | Reusable non-sterile lateral stabilizer for use with Siemens Somatom Sensation CT |