| Primary Device ID | ECMAFUSIONSYNCF10 |
| NIH Device Record Key | 686c0878-af8e-4e2e-9282-4495a6554ff2 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | FUSIONSYNC |
| Version Model Number | F1 |
| Company DUNS | 551455046 |
| Company Name | Chimaera GmbH |
| 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 | 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 | true |
| Phone | +499131691385 |
| info@chimaera.de |
| Device Issuing Agency | Device ID |
|---|---|
| HIBCC | ECMAFUSIONSYNCF10 [Primary] |
| LLZ | System, Image Processing, Radiological |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2018-03-29 |
| Device Publish Date | 2016-07-21 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() FUSIONSYNC 86406127 not registered Dead/Abandoned |
Riverbed Technology, Inc. 2014-09-25 |