| Primary Device ID | D678J12001 |
| NIH Device Record Key | 7f19d349-e801-40a0-866e-1c2f323a4fbb |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ScanX Duo Touch |
| Version Model Number | J1205 |
| Catalog Number | J1200 |
| Company DUNS | 043835081 |
| Company Name | AIR TECHNIQUES, INC. |
| Device Count | 1 |
| DM Exempt | false |
| 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 | false |
| Serial Number | true |
| Manufacturing Date | false |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| HIBCC | D678J12001 [Package] Contains: D678J12050 Package: Box [1 Units] In Commercial Distribution |
| HIBCC | D678J12050 [Primary] |
| MUH | System, X-Ray, Extraoral Source, Digital |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2023-05-01 |
| Device Publish Date | 2023-04-21 |
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