| Primary Device ID | EDET047551 |
| NIH Device Record Key | 11a0ec2d-6010-4eac-9f69-8fe2143fbcd8 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | dx retainer 1000g |
| Version Model Number | 04755 |
| Company DUNS | 343947949 |
| Company Name | DETAX GmbH |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| MRI Safety Status | MR Safe |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | true |
| 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 | EDET047551 [Primary] |
| DYJ | Retainer, Screw Expansion, Orthodontic |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2026-03-16 |
| Device Publish Date | 2026-03-06 |
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