Sodium Electrode

Measuring concentration of Sodium in whole blood, serum, plasma, and diluted urine samples.

Registry build 21.09.26
2manufacturers in China registered for this device type
3catalogue numbers in this listing
4510(k) clearances naming this product code

Who Else Makes It

All of them in Guangdong.

Chinese manufacturers registered for FDA product code JGS
Manufacturer City Province Registered as Device types
Shenzhen Mindray BIO-Medical Electronics Co., Ltd. Shenzhen Guangdong Specification developer 61
Edan Instruments, Inc. Shenzhen Guangdong Contract manufacturer 56

Record

Regulatory record for Sodium Electrode
Listed by Diamond Diagnostics Inc., Hungary
FDA product code JGS
Device type Electrode, Ion Specific, Sodium
Device class Class 2
Regulation 21 CFR 862.1665
Establishment Contract manufacturer, Manufacturer, Exporter
Premarket notification Exempt
Record published 2023-06-05

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, serial number

Catalogue Numbers

Catalogue numbers for Sodium Electrode
Catalogue number Size Status
ME-2102D In distribution
AV-BP0413D In distribution
BM-371037D In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Stat Profile Nova Biomedical Corporation 13
i-STAT Abbott Point OF Care Inc. 9
AU Beckman Coulter, Inc. 8
GEM Premier ChemSTAT PAK Na+,K+,Ca++,Cl-, Glu, Crea, BUN, tCO2, Hct, Lac,pH,pCO2 Instrumentation Laboratory SPA 8
Nova Nova Biomedical Corporation 6
Phoenix Diagnostics, Inc. Phoenix Diagnostics, Inc. 5
Sodium Electrode Roche Diagnostics Gmbh 4
Pointe Scientific, Inc. Horiba Instruments Incorporated 3
Architect Abbott Laboratories 3
Synermed® Infrared Laboratory Systems LLC 3
Phoenix Diagnostics Phoenix Diagnostics, Inc. 2
Sodium Electrode Medica Corp. 2

Showing 12 of 88. All products under Electrode, Ion Specific, Sodium

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K121140 2012-08-22
K102959 2011-01-14
K082462 2009-02-06
K070104 2008-05-07

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