Primary Device ID | 00884838103641 |
NIH Device Record Key | 38575938-2391-4c8a-a240-06da527a2ca8 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | XS-100 X-Ray Tube Assembly |
Version Model Number | 3000-048-52391 |
Catalog Number | 3000-048-52391 |
Company DUNS | 314101218 |
Company Name | Philips Medical Systems DMC GmbH |
Device Count | 1 |
DM Exempt | true |
Pre-market Exempt | true |
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 | 00884838103641 [Primary] |
ITY | Assembly, tube housing, x-ray, diagnostic |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-12-10 |
Device Publish Date | 2020-12-02 |
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