Primary Device ID | 04049957005559 |
NIH Device Record Key | 94973395-a8e8-493d-bea1-fcc7b1477561 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Dornier MedTech |
Version Model Number | Genesis |
Catalog Number | K1041700 |
Company DUNS | 318165065 |
Company Name | Dornier MedTech Systems 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 | true |
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 | 04049957005559 [Primary] |
JAA | System, X-Ray, Fluoroscopic, Image-Intensified |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2018-10-15 |
Device Publish Date | 2018-09-13 |
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