Primary Device ID | 04052682044106 |
NIH Device Record Key | d0e60e6c-1e4f-4ad3-9b4b-951d816c54c9 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Vigilant Software Suite |
Version Model Number | ZK288122 |
Catalog Number | ZK288122 |
Company DUNS | 315654579 |
Company Name | Fresenius Kabi AG |
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 | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04052682044106 [Primary] |
PHC | Infusion Safety Management Software |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-05-30 |
Device Publish Date | 2022-05-20 |
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