Fe

The product is an in vitro diagnostic test intended for the quantitative determination of Iron in serum

Registry build 21.09.26
2manufacturers in China registered for this device type
4catalogue numbers in this listing
1510(k) clearance

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 Fe
Listed by Randox Laboratories Limited, United Kingdom
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, Manufacturer
510(k) K974604
Record published 2016-09-16
Record revised 2018-07-06 (version 3)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Single use Yes
Prescription Prescription only
Supplied as a kit Yes
Label carries lot or batch number, expiry date
Storage Storage environment temperature 2 to 8 °C

Catalogue Numbers

Catalogue numbers for Fe
Catalogue number Size Status
SI2818 In distribution
SI7967 In distribution
SI257 In distribution
SI3821 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Synermed® Infrared Laboratory Systems LLC 5
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
AU Beckman Coulter, Inc. 1

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

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K974604 1998-01-06

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