Medonic M-Series

A fully automatic, 3-part differential, hematology analyzer intended for in vitro diagnostic testing of blood specimens under laboratory conditions.

Registry build 21.09.26
3manufacturers in China registered for this device type
4catalogue numbers in this listing
2510(k) clearances naming this product code

Who Else Makes It

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

Chinese manufacturers registered for FDA product code GKZ
Manufacturer City Province Registered as Device types
VTech Communications Ltd Dongguan Guangdong Contract manufacturer 5
Shenzhen Mindray BIO-Medical Electronics Co., Ltd. Shenzhen Guangdong Specification developer 61
Onechipdx Biotech (Suzhou) Co., Ltd. Suzhou Jiangsu Specification developer 2

Record

Regulatory record for Medonic M-series
Listed by Boule Medical AB, Sweden
FDA product code GKZ
Device type Counter, Differential Cell
Device class Class 2
Regulation 21 CFR 864.5220
Establishment Specification developer, Manufacturer, Exporter
510(k) K083420
Record published 2016-09-17
Record revised 2024-10-08 (version 7)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Label carries manufacturing date, serial number

Catalogue Numbers

Catalogue numbers for Medonic M-series
Catalogue number Size Status
M16C US In distribution
M16M US In distribution
M16S BD ABR US In distribution
M16 US In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
QBC Diagnostics Drucker Diagnostics, LLC 41
Cell-DYN Abbott Laboratories 19
Research and Diagnostic Systems Research AND Diagnostic Systems, Inc. 17
Simultest Becton, Dickinson AND Company 10
BD FACSCanto™ Becton, Dickinson AND Company 10
FACSCanto Becton, Dickinson AND Company 7
BD Multitest Becton, Dickinson AND Company 6
Coulter AcT Beckman Coulter, Inc. 6
BD™ Multi-Check Becton, Dickinson AND Company 6
BD Tritest Becton, Dickinson AND Company 6
Coulter LH Beckman Coulter, Inc. 5
HemoScreen Pixcell Medical Inc. 5

Showing 12 of 245. All products under Counter, Differential Cell

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K083420 2009-02-03
K032214 2004-01-29

Recalls Naming This Product

1 recall names this product by its own identifier, the 510(k) it is cleared under.

Recalls naming the identifiers of Medonic M-series
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Clinical Diagnostic Solutions, Inc. 510(k) number 2020-01-02 Class II Software design A mix-up of autosampler tube positions with a possibility of misidentification of sample results and a risk of operator injury from an exposed aspiration needle. 261 2022-11-03

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