Primary Device ID | 00884838075863 |
NIH Device Record Key | 1fffc3a5-4206-44e6-bf58-85337ffa166f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | 2D Quantitative Analysis |
Version Model Number | 2D Quantitative Analysis R1 |
Catalog Number | 001014 |
Company DUNS | 413819707 |
Company Name | Philips Medical Systems Nederland B.V. |
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 | true |
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 | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00884838075863 [Primary] |
OWB | Interventional Fluoroscopic X-Ray System |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 6 |
Public Version Date | 2019-10-24 |
Device Publish Date | 2017-02-20 |
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