Ready Sensor™ Gold Ph Sensor

Ready Sensor™ pH Biosensor for use on the RapidLab® 248/348/348ex instruments

Registry build 21.09.26
8manufacturers in China registered for this device type
1catalogue number
4recalls 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 Ready Sensor™ Gold pH Sensor
Listed by Siemens Healthcare Diagnostics Inc, United States
FDA product code CGA
Device type Glucose Oxidase, Glucose
Device class Class 2
Regulation 21 CFR 862.1345
Establishment Contract manufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
Record published 2016-09-24
Record revised 2021-11-19 (version 5)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Label carries lot or batch number, expiry date
Storage Storage environment temperature 4 to 25 °C; Special storage condition: Keep away from sunlight

Catalogue Numbers

Catalogue numbers for Ready Sensor™ Gold pH Sensor
Catalogue number Size Per pack Status
10312556 2 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

Recalls

4 of these are 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
2020-08-28 Class II Process control Sporadically inconsistent discrepant (low bias) glucose results on card lot 01-20095-10. Potential exists for a delay in diagnosis of hyperglycemia or unnecessary treatment for hypoglycemia. 463 boxes (50 test cards/box ) 2021-09-09
2016-03-17 Class II Device Design Siemens Healthcare Diagnostics has become aware of N-Acetylcysteine (NAC) and Metamizole (Dipyrone) interference with Trinder and Trinder-like reaction assays. Siemens has confirmed that falsely depressed results may occur on samples drawn 137422 units total 2017-09-25
2015-05-06 Class II Software design D50 and D51 Diagnostic error codes are not functional. 122 devices 2017-08-02
2015-05-06 Class II Software design D50 and D51 diagnostic error codes are not functional. 2713 devices 2017-08-02

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