Algorithm Services

Algorithm Services EK12 V2 is software that analyzes previously recorded electrocardiograms for rhythm and measurements. It processes recordings at least ten seconds long from adults and…

Registry build 21.09.26

Algorithm Services EK12 V2 is software that analyzes previously recorded electrocardiograms for rhythm and measurements. It processes recordings at least ten seconds long from adults and children older than two years, within a host system that generates ECG reports for qualified medical professionals.

The algorithm produces evaluation results for rhythms and measurements, along with annotations of detected rhythm and noise events. Its outputs also identify QRS detection times and classify beats for use in the host system’s ECG reporting workflow.

Listed Item

Algorithm Services EK12 V2

Use Setting

EK12 V2 is used in diagnostic testing facilities or professional medical facilities. It is limited to prerecorded ECG analysis and does not provide the continuous displays, alarms or time-sensitive alerts needed for active patient monitoring.

9manufacturers in China registered for this device type
2catalogue numbers in this listing
34510(k) clearances naming this product code
8recalls on this code

Who Else Makes It

Concentrated in Guangdong (6), Jiangsu (1), Hebei (1). One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code MHX
Manufacturer City Province Registered as Device types
Amphenol Medical Technologies (Dongguan) Co., Ltd. Dongguan Guangdong Contract manufacturer 77
Shenzhen Mindray BIO-Medical Electronics Co., Ltd. Shenzhen Guangdong Specification developer 61
GE Medical Systems (China) Co., Ltd. Wuxi Jiangsu Contract manufacturer 57
Edan Instruments, Inc. Shenzhen Guangdong Contract manufacturer 56
Shenzhen Comen Medical Instruments Co., Ltd. Shenzhen Guangdong Contract manufacturer 24
Contec Medical Systems Co., Ltd. Qinhuangdao Hebei Manufacturer 22
Guangdong Biolight Meditech Co., Ltd. Zhuhai Guangdong Manufacturer 19
Shanghai Draeger Medical Instrument Co., Ltd. Shanghai Shanghai Contract manufacturer 4
General Meditech, Inc. Shenzhen Guangdong Complaint-file establishment 3

Record

Regulatory record for Algorithm Services
Listed by GE Medical Systems Information Technologies, Inc., United States
FDA product code MHX
Device type Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
Device class Class 2
Regulation 21 CFR 870.1025
Establishment Specification developer, Repacker / relabeller, Manufacturer
510(k) K221904
Record published 2017-11-01
Record revised 2025-06-11 (version 5)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Prescription Prescription only
Label carries lot or batch number
Distribution end date 2023-07-31

Catalogue Numbers

Catalogue numbers for Algorithm Services
Catalogue number Size Status
EK12 V2 In distribution
EK12 Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Fukuda Denshi Fukuda Denshi Co., Ltd. 326
Welch Allyn, Inc. Welch Allyn, Inc. 266
Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms) Nihon Kohden Corp. 205
Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms) Nihon Kohden America, Inc. 139
Surveyor Central Mortara Instrument, Inc. 71
Tempus Pro Remote Diagnostic Technologies Ltd. 44
Surveyor S12 Mortara Instrument, Inc. 38
Ultraview Spacelabs Healthcare (Washington), Inc 29
Surveyor S19 Mortara Instrument, Inc. 26
Vital Signs™ AirLife Finland Oy 23
Patient Monitor Edan Instruments, Inc. 22
Telemetry Accessories Philips Medizin Systeme Böblingen GmbH 21

Showing 12 of 589. All products under Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K253277 2026-07-24
K242562 2025-07-09
K222586 2022-12-21
K221904 2022-12-20
K213234 2022-04-12
K213490 2022-04-01
K201941 2020-11-04
K170155 2017-06-06
K141963 2015-02-05
K092369 2010-02-24
K092027 2009-08-28
K091594 2009-07-29
K090702 2009-04-15
K083750 2009-03-23
K080251 2008-06-20
K080157 2008-03-24
K073462 2008-01-11
K073203 2007-11-29
K071073 2007-05-11
K060833 2006-08-01
K051367 2005-06-20
K042642 2004-11-03
K040458 2004-06-03
K033964 2004-01-15
K033492 2003-11-24
K033304 2003-11-12
K033365 2003-11-06
K032369 2003-08-15
K031376 2003-07-16
K022834 2003-05-13
K031320 2003-05-06
K030575 2003-03-21
K030431 2003-02-26
K012915 2002-03-21

Recalls

7 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
2026-04-24 Class II Software design GE HealthCare has become aware of an unlikely situation where potential loss of ECG and SpO2 monitoring involving ApexPro CARESCAPE Telemetry Server (CTS) v5.0 and v6.0, can result from a persistent NO COMM or OFF NETWORK condition at the C 2187 units
2026-04-24 Class II Software design GE HealthCare has become aware of an unlikely situation where potential loss of ECG and SpO2 monitoring involving ApexPro CARESCAPE Telemetry Server (CTS) v5.0 and v6.0, can result from a persistent NO COMM or OFF NETWORK condition at the C 2366 units
2026-04-24 Class II Software design GE HealthCare has become aware of an unlikely situation where potential loss of ECG and SpO2 monitoring involving ApexPro CARESCAPE Telemetry Server (CTS) v5.0 and v6.0, can result from a persistent NO COMM or OFF NETWORK condition at the C 476 units
2026-04-24 Class II Software design GE HealthCare has become aware of an unlikely situation where potential loss of ECG and SpO2 monitoring involving ApexPro CARESCAPE Telemetry Server (CTS) v5.0 and v6.0, can result from a persistent NO COMM or OFF NETWORK condition at the C 14 units
2026-04-24 Class II Software design GE HealthCare has become aware of an unlikely situation where potential loss of ECG and SpO2 monitoring involving ApexPro CARESCAPE Telemetry Server (CTS) v5.0 and v6.0, can result from a persistent NO COMM or OFF NETWORK condition at the C 1249 units
2026-04-24 Class II Software design GE HealthCare has become aware of an unlikely situation where potential loss of ECG and SpO2 monitoring involving ApexPro CARESCAPE Telemetry Server (CTS) v5.0 and v6.0, can result from a persistent NO COMM or OFF NETWORK condition at the C 7 units
2017-07-13 Class II Software Design Change Device does not produce a visual or audible impedance respiration APN alarm when an impedance respiration apnea event occurs. 1,196 (1,176 US; 20 OUS) 2021-04-01
2004-01-27 Not classified Other The potential exists for external electrical noise to be processed as irregular pacing thereby masking potential asystole events. 36 2009-10-05

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