| Primary Device ID | 00850020301539 |
| NIH Device Record Key | cca01553-5b71-4922-8369-9d927c15cabf |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Reliance |
| Version Model Number | 7900 Floor Unit |
| Company DUNS | 080962286 |
| Company Name | HAAG-STREIT USA, INC. |
| Device Count | 1 |
| DM Exempt | false |
| 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 | false |
| 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 | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00850020301539 [Primary] |
| HMF | Stand, Instrument, Ac-Powered, Ophthalmic |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2025-05-02 |
| Device Publish Date | 2025-04-24 |