Synchron

SYNCHRON Systems Phosphorus Reagent

Registry build 21.09.26
2manufacturers in China registered for this device type
2catalogue numbers in this listing
1510(k) clearance
1recall

Who Else Makes It

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

Chinese manufacturers registered for FDA product code CEO
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 Synchron
Listed by Beckman Coulter, Inc., United States
FDA product code CEO
Device type Phosphomolybdate (Colorimetric), Inorganic Phosphorus
Device class Class 1
Regulation 21 CFR 862.1580
Establishment Contract manufacturer, Specification developer, Manufacturer, Exporter
Record published 2016-08-24
Record revised 2023-08-28 (version 5)

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, manufacturing date

Catalogue Numbers

Catalogue numbers for Synchron
Catalogue number Size Status
467868 In distribution
A09426 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Biobase Biobase Biodustry(Shandong)Co., Ltd. 13
Synermed® Infrared Laboratory Systems LLC 7
Pointe Scientific, Inc. Phosphorus Horiba Instruments Incorporated 6
Carolina Liquid Chemistries Corp.® Phosphorus Reagent KIT AU-218 Carolina Liquid Chemistries 5
JAS Diagnostics Drew Scientific, Ltd. 4
Pointe Scientific, Inc. Horiba Instruments Incorporated 4
Phosphate (Inorganic) ver.2 Roche Diagnostics Gmbh 3
Inorganic Phosphorous (Phos) Randox Laboratories Limited 3
Pointe Phosphorus Reagent Horiba Instruments Incorporated 2
Architect Abbott Medical 2
Architect Abbott Laboratories 2
Architect Abbott Ireland 2

Showing 12 of 40. All products under Phosphomolybdate (Colorimetric), Inorganic Phosphorus

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K041643 2004-08-18

Recalls Naming This Product

1 recall names this product by its own identifier, the UDI on its label.

Recalls naming the identifiers of Synchron
Recalled by Identified by Initiated FDA class Root cause Reason Quantity
Beckman Coulter, Inc. UDI-DI 2025-09-03 Class II Unknown/Undetermined by firm Specific SYNCHRON Systems Modular Chemistry Phosphorus (PHOSm REF 467868) reagent lots may fail calibration before the lot expiration date which causes a delay in obtaining patient results. 2146 units

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