Primary Device ID | 04052682058912 |
NIH Device Record Key | e43839d3-011e-48bd-8d7a-017d61e43e2c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | AGILIA DUO US |
Version Model Number | Z073607 |
Catalog Number | Z073607 |
Company DUNS | 315654579 |
Company Name | Fresenius Kabi AG |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Unsafe |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
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 | true |
OTC Over-The-Counter | false |
Phone | (888) 391-6300 |
communications.USA@fresenius-kabi.com | |
Phone | (888) 391-6300 |
communications.USA@fresenius-kabi.com | |
Phone | (888) 391-6300 |
communications.USA@fresenius-kabi.com | |
Phone | (888) 391-6300 |
communications.USA@fresenius-kabi.com | |
Phone | (888) 391-6300 |
communications.USA@fresenius-kabi.com | |
Phone | (888) 391-6300 |
communications.USA@fresenius-kabi.com | |
Phone | (888) 391-6300 |
communications.USA@fresenius-kabi.com | |
Phone | (888) 391-6300 |
communications.USA@fresenius-kabi.com | |
Phone | (888) 391-6300 |
communications.USA@fresenius-kabi.com | |
Phone | (888) 391-6300 |
communications.USA@fresenius-kabi.com | |
Phone | (888) 391-6300 |
communications.USA@fresenius-kabi.com | |
Phone | (888) 391-6300 |
communications.USA@fresenius-kabi.com | |
Phone | (888) 391-6300 |
communications.USA@fresenius-kabi.com | |
Phone | (888) 391-6300 |
communications.USA@fresenius-kabi.com | |
Phone | (888) 391-6300 |
communications.USA@fresenius-kabi.com | |
Phone | (888) 391-6300 |
communications.USA@fresenius-kabi.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04052682058912 [Primary] |
MRZ | Accessories, Pump, Infusion |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-10-26 |
Device Publish Date | 2022-10-18 |
00810020440591 - AMICUS Separator Legacy Software | 2024-04-04 Software version for AMICUS Separator Legacy Device |
00810020440607 - AMICUS Separator Life Extension Software | 2024-04-04 Software version for AMICUS Separator Life Extension Device |
04250273750164 - Volumat™ Line | 2024-03-29 IV administration set for infusion pumps |
04250273750218 - Volumat™ Line | 2024-03-29 IV administration set for infusion pumps |
04250273750287 - Volumat™ Line | 2024-03-29 IV administration set for infusion pumps |
04250273750294 - Volumat™ Line | 2024-03-29 IV administration set for infusion pumps |
10810020441632 - Amicus Apheresis Kit - Functionally Closed Single Needle with PAS Spike and Dual | 2024-02-01 For Extended Platelet Storage with Plasma and Red Blood Cell Collection. For Platelet Storage in Plasma or Platelet Additive Sol |
10810020441649 - Amicus Apheresis Kit - Functionally Closed Double Needle with PAS Spike and Dual | 2024-02-01 For Extended Platelet Storage and Plasma Collection. For Platelet Storage in Plasma or Platelet Additive Solution Plus Plasma. F |