FUJIFILM Wako Pure Chemical Corporation Diagnostics Design Office (Amagasaki)

FDA Device Registration & Listing · Amagasaki-shi Hyogo, JP · Registration 3003419906

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3003419906
FEI Number
3003419906
Entity Name
FUJIFILM Wako Pure Chemical Corporation Diagnostics Design Office (Amagasaki)
City/State/Country
Amagasaki-shi Hyogo, JP
Establishment Address
6-1 Takata-cho, Amagasaki-shi Hyogo 661-0963, JP
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
FUJIFILM Wako Pure Chemical Corporation (Owner Number: 8030234)
Owner / Operator Contact Address
1-2 Doshomachi 3-Chome, Chuo-Ku, JP-27 540-8605, JP
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

L-Type HDL-C Reagent NEFA Linearity Material Complement Control HR SERIES NEFA-HR2 Solvent A HR SERIES NEFA-HR2 Solvent B HR SERIES NEFA-HR2 Color Reagent B HR SERIES NEFA-HR2 Color Reagent A Autokit Micro Albumin Control Set Autokit Micro Albumin Calibrator Set Autokit Micro Albumin Microalbumin Controls Alinity c Microalbumin Calibrators Alinity c Microalbumin Reagent Kit Microalbumin Calibrators Microalbumin Alinity c Microalbumin Controls uTASWako AFP-L3 Sample Dilution Buffer uTASWako DCP Control L and H uTASWako AFP-L3 Immunological Test System uTASWako AFP-L3 Control L and H uTASWako i30 Immunoanalyzer System uTASWako DCP Calibrator Set uTASWako DCP Immunological Test System uTASWako AFP-L3 Calibrator Set uTASWako Chip Cassette uTASWako Wash Solution Wako HDL-C/LDL-C Calibrator

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
LBR Ldl & Vldl Precipitation, Hdl Clinical Chemistry Class 1 862.1475 2007-02-23
JIS Calibrator, Primary Clinical Chemistry Class 2 862.1150 2007-02-23
JJX Single (Specified) Analyte Controls (Assayed And Unassayed) Clinical Chemistry Class 1 862.1660 2009-02-09
JJX Single (Specified) Analyte Controls (Assayed And Unassayed) Clinical Chemistry Class 1 862.1660 2007-12-18
JLH Titrimetric, Fatty Acids Clinical Chemistry Class 1 862.1290 2007-01-18
JIS Calibrator, Primary Clinical Chemistry Class 2 862.1150 2006-03-01
JIQ Turbidimetric Method, Protein Or Albumin (Urinary, Non-Quant.) Clinical Chemistry Class 1 862.1645 2006-03-01
JJX Single (Specified) Analyte Controls (Assayed And Unassayed) Clinical Chemistry Class 1 862.1660 2006-03-01
JJX Single (Specified) Analyte Controls (Assayed And Unassayed) Clinical Chemistry Class 1 862.1660 2011-02-28
OAU Des-Gamma-Carboxy-Prothrombin (Dcp), Risk Assessment, Hepatocellular Carcinoma Immunology Class 2 866.6030 2011-02-28
NSF Test, Alpha Fetoprotein L3 Subfraction (Afp-L3%), For Hepatocellular Carcinoma Risk Assessment Immunology Class 2 866.6030 2011-02-28
JIT Calibrator, Secondary Clinical Chemistry Class 2 862.1150 2011-02-28
OUE Micro Total Analysis Instrument System Clinical Chemistry Class 2 862.2570 2011-02-28
JIS Calibrator, Primary Clinical Chemistry Class 2 862.1150 2010-11-05

Official Correspondent

No official correspondent registered.

US Agent Details

Randy Vader Business: FUJIFILM Healthcare Americas Corporation Email: randy.vader@fujifilm.com Phone: (360) 3566821

Related Public Records

Same Entity

FUJIFILM Wako Pure Chemical Corporation
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3003522182 FUJIFILM Healthcare Manufacturing Corporation MIE Office Komono-cho, Mie-gun, JP

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K103744 Quantimetrix Corp. DROPPER A1C DIABETES CONTROL 2011-05-12
K981281 Roche Diagnostics GmbH ELECSYS CALCHECK FERRITIN 1998-04-24
K981278 Roche Diagnostics GmbH ELECSYS CALCHECK CA 125II 1998-04-23
K143687 Siemens Healthcare Diagnostics, Inc. ADVIA Centaur Follicle Stimulating Hormone (FSH) Master Curve Material, ADVIA Centaur FT4 Master Curve Material, ADVIA Centaur T4 Master Curve Material, ADVIA Centaur T3 Master Curve Material 2015-07-17
K143376 Siemens Healthcare Diagnostics, Inc. ADIVA Centaur Progesterone Master Curve Material (MCM), ADIVA Centaur Ferritin Master Curve Material 2014-12-23

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0023-2007 Abbott Diagnostic International, Ltd. Carr 2 Km 58.0 Cruce Davila 2
Abbott AxSYM system FSH Master Calibrators (LN 7A60-30), for in vitro diagnostic use.
Z-0033-2022 Sentinel CH SpA Via Robert Koch 2
Alinity c CRP Vario Cardiac High Sensitivity Calibrator Kit (ref 07P5605) - Product Usage: use in the calibration of the Alinity c CRP Vario assay, Cardiac CRP high sensitivity method [Cardiac CRP], on the Alinity c analyzer.
Z-0007-2008 Tosoh Bioscience Inc 1
4 glass vials per box. 2/4ml vials of Sample Diluting Solution & 2/2ml vials of Calibration Verification Material. BetaHCG Calibration Verification Test Set, in vitro diagnostic.
Z-0024-2007 Abbott Diagnostic International, Ltd. Carr 2 Km 58.0 Cruce Davila 2
FSH Calibrators (LN 9C06-01), for in vitro diagnostic use.
Z-0024-2015 Siemens Healthcare Diagnostics, Inc. 2
Dimension Vista Mass CKMB Isoenzyme Calibrator (MMB CAL) an in vitro diagnostic product for the calibration of Creatine Kinase MB Isoenzyme (MMB) method on the Dimension Vista System.

Similar Registrations

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3003522182 FUJIFILM Healthcare Manufacturing Corporation MIE Office Komono-cho, Mie-gun, JP
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3003419906. Last updated year: 2026. Please use registration number 3003419906 when referencing this establishment in official correspondence.
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