| Primary Device ID | 00812559010221 |
| NIH Device Record Key | 0485384d-97b9-44ba-9b14-e53aaeed1d1b |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | CT210 Contact Tonometer |
| Version Model Number | 12598 |
| Company DUNS | 126650253 |
| Company Name | REICHERT, 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 | 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 | 1-888-849-8955 |
| reichert.information@ametek.com | |
| Phone | 1-888-849-8955 |
| reichert.information@ametek.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00812559010221 [Primary] |
| HKY | Tonometer, Manual |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-09-22 |
| 00812559012485 - Ocu-Film® +" | 2025-08-25 |
| 00812559012492 - Ocu-Film® +" | 2025-08-22 |
| 00812559010238 - Ultramatic RX Master Phoropter | 2025-08-20 |
| 00812559010269 - Ultramatic RX Master Phoropter | 2025-08-20 |
| 00812559010290 - Illuminated Phoropter | 2025-08-20 |
| 00812559010320 - Illuminated Phoropter | 2025-08-20 |
| 00812559010559 - TF50 Trial Frame | 2025-08-20 |
| 00812559010566 - TS75 Trial Lens | 2025-08-20 |