| Primary Device ID | 00842000100218 |
| NIH Device Record Key | d4d0c364-0001-4d09-af14-180908f59a49 |
| Commercial Distribution Discontinuation | 2016-12-01 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | Merge Hemo System |
| Version Model Number | Nellcor PDM + 10.0.4 |
| Company DUNS | 065626069 |
| Company Name | MERGE HEALTHCARE SOLUTIONS INC. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Safe |
| 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 | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00842000100218 [Primary] |
| DQK | Computer, Diagnostic, Programmable |
| 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 | 2016-12-01 |
| 00842000100270 | Merge Hemo System [Masimo PDM + 9.40.3 Patch 1] Virtual UDI. |
| 00842000100263 | Merge Hemo System [Masimo PDM + 9.40.4] Virtual UDI. |
| 00842000100256 | Merge Hemo System [Masimo PDM + 10.0.3 Patch 1] Virtual UDI. |
| 00842000100249 | Merge Hemo System [Masimo PDM + 10.0.4] Virtual UDI. |
| 00842000100218 | Merge Hemo System [Nellcor PDM + 10.0.4] Virtual UDI. |
| 00842000100201 | Merge Hemo System [Nellcor PDM + 10.0.3 Patch 1]. Virtual UDI. |
| 00842000100195 | Merge Hemo System [Nellcor PDM + 9.40.4]. Virtual UDI. |
| 00842000100188 | Merge Hemo System [Nellcor PDM + 9.40.3 Patch 1] Virtual UDI. |