Primary Device ID | 04056869009049 |
NIH Device Record Key | 46a5c7d4-aeac-44eb-949d-ea8e6c286ca5 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Cios Connect |
Version Model Number | 10308193 |
Company DUNS | 313217003 |
Company Name | Siemens Healthcare 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 | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04056869009049 [Primary] |
OXO | Image-intensified fluoroscopic x-ray system, mobile |
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 | 2016-09-24 |
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Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
CIOS CONNECT 79151938 4701995 Live/Registered |
Siemens Healthcare GmbH 2014-08-04 |