Primary Device ID | 00884838088115 |
NIH Device Record Key | 6000a5d3-8134-4b6b-b5a8-62d90989d4ff |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Ingenia Elition X |
Version Model Number | 781358 |
Company DUNS | 413819707 |
Company Name | Philips Medical Systems Nederland B.V. |
Device Count | 1 |
DM Exempt | true |
Pre-market Exempt | false |
MRI Safety Status | MR Safe |
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 | true |
OTC Over-The-Counter | false |
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Device Issuing Agency | Device ID |
---|---|
GS1 | 00884838088115 [Primary] |
LNH | System, nuclear magnetic resonance imaging |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2019-05-03 |
Device Publish Date | 2018-04-25 |
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