Primary Device ID | 04086000860888 |
NIH Device Record Key | af6b771a-86be-474a-92f9-374e24a626de |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | COMPOGUARD Advance Basic |
Version Model Number | 9029741 |
Catalog Number | 9029741 |
Company DUNS | 315654579 |
Company Name | Fresenius Kabi AG |
Device Count | 1 |
DM Exempt | false |
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 | true |
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 | 04086000860888 [Primary] |
KSQ | Device, Blood Mixing And Blood Weighing |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-11-07 |
Device Publish Date | 2024-10-30 |
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