Primary Device ID | 00884838083325 |
NIH Device Record Key | a976fac9-f743-40d2-9fa3-f0baaa4b7626 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Brilliance CT |
Version Model Number | 728231 |
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 | 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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00884838083325 [Primary] |
JAK | System, x-ray, tomography, computed |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2019-12-03 |
Device Publish Date | 2017-01-15 |
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