| Primary Device ID | 06430033850565 |
| NIH Device Record Key | abcb24ee-8c10-42b8-893e-17f38d8df3b9 |
| Commercial Distribution Discontinuation | 2016-12-01 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | Icare tonometer probes |
| Version Model Number | TP01s |
| Company DUNS | 651755092 |
| Company Name | ICARE FINLAND OY |
| 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 | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | true |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 06430033850565 [Primary] |
| HKX | Tonometer, Ac-Powered |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-12-01 |
| 06430033851463 - iCare IC200 | 2023-06-28 iCare IC200 (with Quick Measure feature) |
| 06430033851456 - iCare HOME2 | 2022-02-16 |
| 06430033850985 - Icare PATIENT | 2020-05-19 Icare PATIENT |
| 06430033851074 - Icare HOME tonometer | 2020-05-19 |
| 06430033850947 - Probes for HOME | 2020-05-12 Sales package 20pcs of TP022 probes |
| 16430033850623 - Probes for HOME | 2020-05-12 Sales package 50pcs |
| 06430033850626 - Probes for HOME | 2020-05-12 Single unit blister package |
| 06430033850961 - Icare CLINIC | 2020-02-13 Icare CLINIC |