Primary Device ID | 00884838093010 |
NIH Device Record Key | 84715adb-c35c-4edd-a754-9a1004423d65 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Philips MRC 800 CPO |
Version Model Number | 9890-000-30091 |
Catalog Number | 9890-000-30091 |
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 | 00884838093010 [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 | 2019-02-11 |
Device Publish Date | 2019-01-11 |
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