Yumizen C1200 Transferrin

GUDID 03610230007419

HORIBA ABX SAS

Transferrin IVD, kit, nephelometry/turbidimetry Transferrin/transferrin isoform IVD, kit, nephelometry/turbidimetry Transferrin/transferrin isoform IVD, kit, nephelometry/turbidimetry Transferrin/transferrin isoform IVD, kit, nephelometry/turbidimetry Transferrin/transferrin isoform IVD, kit, nephelometry/turbidimetry Transferrin/transferrin isoform IVD, kit, nephelometry/turbidimetry Transferrin/transferrin isoform IVD, kit, nephelometry/turbidimetry Transferrin/transferrin isoform IVD, kit, nephelometry/turbidimetry Transferrin/transferrin isoform IVD, kit, nephelometry/turbidimetry Transferrin/transferrin isoform IVD, kit, nephelometry/turbidimetry Transferrin/transferrin isoform IVD, kit, nephelometry/turbidimetry Transferrin/transferrin isoform IVD, kit, nephelometry/turbidimetry Transferrin/transferrin isoform IVD, kit, nephelometry/turbidimetry Transferrin/transferrin isoform IVD, kit, nephelometry/turbidimetry Transferrin/transferrin isoform IVD, kit, nephelometry/turbidimetry Transferrin/transferrin isoform IVD, kit, nephelometry/turbidimetry Transferrin/transferrin isoform IVD, kit, nephelometry/turbidimetry Transferrin/transferrin isoform IVD, kit, nephelometry/turbidimetry
Primary Device ID03610230007419
NIH Device Record Keyf003850d-8676-4693-80e1-412c1cc1277d
Commercial Distribution StatusIn Commercial Distribution
Brand NameYumizen C1200 Transferrin
Version Model Number1300023889
Company DUNS273647420
Company NameHORIBA ABX SAS
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS103610230007419 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

DDGTransferrin, Antigen, Antiserum, Control

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-05-14
Device Publish Date2020-05-06

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03610230004937 - ABX PENTRA GGT CP2023-07-06
03610230004944 - ABX PENTRA LIPASE CP2023-07-06
03610230004975 - ABX PENTRA CHOLESTEROL CP2023-07-06
03610230004982 - ABX PENTRA BILIRUBIN, DIRECT CP2023-07-06
03610230004999 - ABX PENTRA HDL DIRECT CP2023-07-06

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