Primary Device ID | 14086000101384 |
NIH Device Record Key | 1a2f73a2-641a-4c5e-8731-27cccf1bf083 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Fenwal AMICUS Double Needle Advanced Kit |
Version Model Number | 4R2354 |
Catalog Number | 4R2354 |
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 | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Special Storage Condition, Specify | Between 0 and 0 *Store at Controlled Room Temperature. Protect from freezing. Avoid excessive heat. |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04086000101387 [Primary] |
GS1 | 14086000101384 [Package] Contains: 04086000101387 Package: Carton [3 Units] In Commercial Distribution |
GKT | Separator, Automated, Blood Cell, Diagnostic |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-09-02 |
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