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 |