eGLU, 15ct., CCPlus Home

Catalogue number REF 4755, listed by Polymer Technology Systems, United States, under Glucose Oxidase, Glucose. 8 manufacturers in China are registered for this product code.

Registry build 21.09.26
8manufacturers in China registered for this device type
1catalogue number
4510(k) clearances naming this product code
3recalls on this code

Who Else Makes It

Concentrated in Guangdong (3), Zhejiang (2), Jiangsu (1). 4 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code CGA
Manufacturer City Province Registered as Device types
Acon Biotech (Hangzhou) Co., Ltd. Hangzhou Zhejiang Contract manufacturer 29
Dongguan BAO Kang Dian ZI KE JI Limited Dongguan Guangdong Contract manufacturer 24
Flextronics Industrial (Shenzhen) Co., Ltd. Shenzhen Guangdong Contract manufacturer 5
Yasee Biomedical Inc Qingdao Shandong Contract manufacturer 5
Jiangsu NEW Pentastar Medical Products Co., Ltd. Changzhou Jiangsu Exporter 146
Vivachek Biotech (Hangzhou) Co., Ltd. Hangzhou, Zhuji Zhejiang Contract manufacturer 21
Shenzhen Yuwen E-Commerce Co., Ltd. Shenzhen Guangdong Repacker / relabeller 19
Tianjin Empecs Medical Device Co., Ltd. Tianjin Tianjin Contract manufacturer 8

Record

Regulatory record for eGLU, 15ct., CCPlus Home
Listed by Polymer Technology Systems, United States
FDA product code CGA
Device type Glucose Oxidase, Glucose
Device class Class 2
Regulation 21 CFR 862.1345
Establishment Complaint-file establishment, Manufacturer
510(k) K140068
Record published 2023-06-20

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Single use Yes
Over the counter Yes
Label carries lot or batch number, expiry date
Storage Special storage condition: Keep away from sunlight Keep dry; Storage environment temperature 68 to 86 °F; Storage environment temperature 20 to 30 °C

Catalogue Numbers

Catalogue numbers for eGLU, 15ct., CCPlus Home
Catalogue number Size Per pack Status
REF 4755 15 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
i-STAT Abbott Point OF Care Inc. 48
YSI Incorporated YSI Incorporated 34
Auvon Shenzhen Yuwen E-Commerce Co., Ltd. 28
Stat Profile Nova Biomedical Corporation 17
Fora Fora Care Inc. 13
TRUEtrack Trividia Health, Inc. 12
JAS Diagnostics Drew Scientific, Ltd. 11
StatStrip Nova Biomedical Corporation 9
Gluc-PAP Randox Laboratories Limited 8
Nova Primary Nova Biomedical Corporation 8
Synermed® Infrared Laboratory Systems LLC 7
Prodigy No Coding Blood Glucose Test Strips Prodigy Diabetes Care, LLC 7

Showing 12 of 215. All products under Glucose Oxidase, Glucose

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K151530 2015-07-07
K142302 2014-10-02
K013068 2001-11-20
K972669 1998-01-22

Recalls Naming This Product

4 recalls name this product by its own identifiers, the 510(k) it is cleared under.

Recalls naming the identifiers of eGLU, 15ct., CCPlus Home
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Polymer Technology Systems 510(k) number 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
Polymer Technology Systems 510(k) number 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
Polymer Technology Systems 510(k) number 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 2020-07-06
Polymer Technology Systems 510(k) number 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

Recalls

1 of these is Class II. Class II means a temporary or reversible health consequence. Class III is unlikely to cause harm at all → typically a labelling or documentation fault. 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
2022-08-16 Class III Labeling Change Control Incorrect instructions for use were packaged into the final product.
2019-01-16 Class II Device Design Some lots of test strips do not fit tightly into the optical block, and may fall out during analysis, which could lead to an incorrect result being displayed 67643 total 2020-06-24
2009-08-04 Not classified Other Possible under recovery of cholesterol, HDL and glucose. A loss of recoverable cholesterol and HDL cholesterol is a manageable to moderate health risk. The clinical applications analysis shows that lot 1891 shows such a loss of activity. A 962 2010-10-20

PMA Approvals

A premarket approval is the full Class III route, granted on clinical evidence rather than on equivalence to an existing device. It is the highest regulatory bar a device of this type can clear.

FDA premarket approvals naming this product code
PMA number Decision Trade name Approved to
P990026 2002-02-04 CYGNUS GLUCOWATCH AUTOMATIC GLUCOSE BIOGRAPHER Animas Corp.

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