CardioChek® Plus Professional Analyzer, Refurbished

Catalogue number 2702, listed by Polymer Technology Systems, United States, under Ldl & Vldl Precipitation, Hdl. 3 manufacturers in China are registered for this product code.

Registry build 21.09.26
3manufacturers in China registered for this device type
1catalogue number
1510(k) clearance

Who Else Makes It

Concentrated in Zhejiang (2), Guangxi (1). One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code LBR
Manufacturer City Province Registered as Device types
Acon Biotech (Hangzhou) Co., Ltd. Hangzhou Zhejiang Contract manufacturer 29
Urit Medical Electronic Co., Ltd. Guilin Guangxi Contract manufacturer 28
Hangzhou Lysun Biotechnology Co., Ltd. Hangzhou Zhejiang Manufacturer 22

Record

Regulatory record for CardioChek® Plus Professional Analyzer, Refurbished
Listed by Polymer Technology Systems, United States
FDA product code LBR
Device type Ldl & Vldl Precipitation, Hdl
Device class Class 1
Regulation 21 CFR 862.1475
Establishment Complaint-file establishment, Manufacturer
Record published 2016-07-15
Record revised 2023-10-18 (version 7)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Prescription Prescription only
Over the counter Yes
Label carries manufacturing date, serial number
Storage Storage environment humidity 20 to 80 % RH; Storage environment temperature 10 to 40 °C; Storage environment temperature 50 to 104 °F; Special storage condition: Keep away from sunlight.; Special storage condition: Keep dry.

Catalogue Numbers

Catalogue numbers for CardioChek® Plus Professional Analyzer, Refurbished
Catalogue number Size Status
2702 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Pointe Scientific, Inc. Horiba Instruments Incorporated 11
Synermed® Infrared Laboratory Systems LLC 4
LDL-Cholesterol Gen.3 Roche Diagnostics Gmbh 3
L-Type HDL-C Reagent 2 Fujifilm Wako Pure Chemical Corporation 2
Teco Diagnostics Direct HDL Cholesterol Reagent Kit TC-Matrix Teco Diagnostics 2
N-geneous LDL Cholesterol Reagent (R1) Sekisui Diagnostics, LLC 2
N-geneous LDL Cholesterol Reagent (R2) Sekisui Diagnostics, LLC 2
PTS Panels® HDL Cholesterol Test Strips Polymer Technology Systems 2
Teco Diagnostics HDL Cholesterol Reagent Set Teco Diagnostics 2
CardioChek Henry Schein, Inc. 2
L-Type HDL-C Reagent 1 Fujifilm Wako Pure Chemical Corporation 2
Carolina Liquid Chemistries Corp.® CLC720 HDL RGT KIT Product No. ST616 Carolina Liquid Chemistries 1

Showing 12 of 47. All products under Ldl & Vldl Precipitation, Hdl

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K990247 1999-05-28

Recalls Naming This Product

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

Recalls naming the identifiers of CardioChek® Plus Professional Analyzer, Refurbished
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Polymer Technology Systems UDI-DI 2019-12-02 Class II Device Design One brand of batteries have a small dimensional difference in the negative button terminal, which, when the batteries are inserted incorrectly, can create the possibility for the battery terminals to make reverse contact. This reverse cont 44,448 total 2020-07-06

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