Atellica CH Tibc

Total Iron Binding Capacity ( TIBC) Atellica CH - RGT 800T

Registry build 21.09.26
2manufacturers in China registered for this device type
1catalogue number
2recalls on this code

Who Else Makes It

Concentrated in Jilin (1), Shandong (1).

Chinese manufacturers registered for FDA product code JMO
Manufacturer City Province Registered as Device types
Dirui Industrial Co., Ltd. Changchun Jilin Contract manufacturer 84
Biobase Biodustry(Shandong)Co., Ltd. Jinan Shandong Manufacturer 70

Record

Regulatory record for Atellica CH Tibc
Listed by Siemens Healthcare Diagnostics Inc, United States
FDA product code JMO
Device type Ferrozine (Colorimetric) Iron Binding Capacity
Device class Class 1
Regulation 21 CFR 862.1415
Establishment Contract manufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
510(k) K000781
Record published 2020-09-24
Record revised 2021-11-18 (version 2)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Label carries lot or batch number, expiry date
Storage Storage environment temperature 2 to 8 °C

Catalogue Numbers

Catalogue numbers for Atellica CH Tibc
Catalogue number Size Status
11097525 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Synermed® Infrared Laboratory Systems LLC 5
Fe Randox Laboratories Limited 4
Uibc-SL Sekisui Diagnostics, LLC 4
Biobase Biobase Biodustry(Shandong)Co., Ltd. 3
Synchron Beckman Coulter, Inc. 3
Total Iron-Binding Capacity 2 (TIBC_2) Randox Laboratories Limited 3
Iron (Total) Sekisui Diagnostics, LLC 2
Pointe Scientific, Inc. Horiba Instruments Incorporated 2
K-Assay® Uibc Reagent Kamiya Biomedical Company LLC 2
Total-Iron Binding Capacity (Tibc) Randox Laboratories Limited 2
Iron (Fe) Randox Laboratories Limited 2
Direct Tibc Reagent Medtest DX 1

Showing 12 of 29. All products under Ferrozine (Colorimetric) Iron Binding Capacity

Recalls

1 of these is Class III. Class III is unlikely to cause harm at all → typically a labelling or documentation fault. Volume alone is not a quality signal: a manufacturer that ships more recalls more.

Recalls referencing this product code
Initiated FDA class Root cause Reason Quantity Closed
2012-12-20 Class III Process design The analytical sensitivity claim of 6 ug/dL (1.1 umol/L) in the Instructions for Use (IFU) is no longer valid. Siemens is conducting a voluntary corrective action for Dimension Total Iron Binding Capacity (IBCT) to modify the analytical se 19, 503 cartons 2014-08-26
2009-12-16 Not classified Nonconforming Material/Component Test produces falsely elevated IBCT results and Abnormal Reaction test report messages on heparinized plasma samples. unknown – all lots involved 2010-10-25

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer