Synchron

Lipase Reagent (LIP 2 x 60)

Registry build 21.09.26
2manufacturers in China registered for this device type
1catalogue number
1recall

Who Else Makes It

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

Chinese manufacturers registered for FDA product code CHI
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 CHI
Device type Lipase-Esterase, Enzymatic, Photometric, Lipase
Device class Class 1
Regulation 21 CFR 862.1465
Establishment Contract manufacturer, Specification developer, Manufacturer, Exporter
Premarket notification Exempt
Record published 2016-08-24
Record revised 2023-07-06 (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, manufacturing date

Catalogue Numbers

Catalogue numbers for Synchron
Catalogue number Size Status
476851 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Biobase Biobase Biodustry(Shandong)Co., Ltd. 7
Lipase (LPS) Randox Laboratories Limited 4
Carolina Liquid Chemistries Corp.® Lipase Reagent KIT ST621 Carolina Liquid Chemistries 4
Lipase colorimetric assay Roche Diagnostics Gmbh 3
Architect Abbott Ireland 2
Vitros Ortho-Clinical Diagnostics, Inc. 2
Pointe Scientific, Inc. Lipase-Color Horiba Instruments Incorporated 2
Alinity Abbott Ireland 2
Architect Abbott Laboratories 1
Dimension Vista® Flex® reagent cartridge Lipl Siemens Healthcare Diagnostics Inc 1
MedTest Dx, Inc. Lipase (Colorimetric) Medtest DX 1
Lipase NG OC Reagent Kit Sentinel CH. SPA 1

Showing 12 of 28. All products under Lipase-Esterase, Enzymatic, Photometric, Lipase

Recalls

The FDA has not published a severity grade for these. 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
2004-10-25 Not classified Other Beckman Coulter has confirmed that occasionally a cuvette may be skipped during the SYNCHRON Lipase Wash (LIWA) procedure. If this occurs, there is the potential for carryover into the SYNCHRON Lipase (LIPA) assay, resulting ina substantial 6,698 2005-06-17

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