Architect

Lipase

Registry build 21.09.26
2manufacturers in China registered for this device type
1catalogue number
1510(k) clearance
2recalls on this code

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 Architect
Listed by Abbott Laboratories, United States
FDA product code CHI
Device type Lipase-Esterase, Enzymatic, Photometric, Lipase
Device class Class 1
Regulation 21 CFR 862.1465
Establishment Specification developer, Complaint-file establishment, Manufacturer, Exporter
Premarket notification Exempt
Record published 2018-07-31
Record revised 2024-02-21 (version 3)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Prescription Prescription only
Supplied as a kit Yes
Label carries lot or batch number, expiry date
Storage Handling environment temperature up to 29 °C; Storage environment temperature 2 to 8 °C

Catalogue Numbers

Catalogue numbers for Architect
Catalogue number Size Status
7D80-31 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
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
Lipase colorimetric Roche Diagnostics Gmbh 1

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

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K884596 1988-12-06

Recalls

1 of these is Class II. Class II means a temporary or reversible health consequence. 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
2014-04-07 Class II Labeling Change Control Package inserts have incorrect SmartWash parameters for Triglyceride. 11916 units 2015-04-01
2007-06-01 Not classified Other Lipase results are falsely elevated when a
MULTIGENT Acetaminophen test is pipetted immediately before a Lipase test from the same sample cup or tube on the ARCHITECT c8000.
7260 2012-04-05

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