Infinity Mcable-Nellcor Oximax

Catalogue number MS20668, listed by Draeger Medical Systems, Inc., United States, under Oximeter. 70 manufacturers in China are registered for this product code.

Registry build 21.09.26
70manufacturers in China registered for this device type
1catalogue number
3510(k) clearances naming this product code

Who Else Makes It

Concentrated in Guangdong (46), Jiangsu (7), Beijing (5). 10 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code DQA
Manufacturer City Province Registered as Device types
Amphenol Medical Technologies (Dongguan) Co., Ltd. Dongguan Guangdong Contract manufacturer 77
Tianjin Choice Medical Device Co., Ltd. Tianjin Tianjin Contract manufacturer 12
Taijia Medical Electronics (Shenzhen) Co., Ltd. Shenzhen Guangdong Contract manufacturer 10
EMI (Dongguan) Asia Limited Dongguan Guangdong Contract manufacturer 9
Wuhan Strong Electronics Wuhan Hubei Contract manufacturer 6
Regent Electron Suzhou Co., Ltd. Wujiang Jiangsu Contract manufacturer 5
Dongguan Ruibaolian Medical Science & Technology Co., Ltd. Dongguan Guangdong Contract manufacturer 4
Dongguan Kepler Special Cabling Company Limited Dongguan Guangdong Contract manufacturer 3
Measurement Specialties Chengdu Chengdu Sichuan Contract manufacturer 3
Beijing Kingst Commercial & Trade Co., Ltd. Beijing Beijing Contract manufacturer 2
Suzhou Meccan Import and Export Corp. Suzhou Jiangsu Contract manufacturer 71
Shenzhen Mindray BIO-Medical Electronics Co., Ltd. Shenzhen Guangdong Specification developer 61

Showing 12 of 70. All 70 manufacturers in China registered for Oximeter

Record

Regulatory record for Infinity Mcable-Nellcor Oximax
Listed by Draeger Medical Systems, Inc., United States
FDA product code DQA
Device type Oximeter
Device class Class 2
Regulation 21 CFR 870.2700
Establishment Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer
510(k) K113798
Record published 2015-10-24
Record revised 2018-07-06 (version 3)

Specifications

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

Catalogue Numbers

Catalogue numbers for Infinity Mcable-Nellcor Oximax
Catalogue number Size Status
MS20668 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Unimed Unimed Medical Supplies Inc 2,838
APK APK Technology Co., Ltd. 2,678
ChoiceMMed Beijing Choice Electronic Technology Co., Ltd. 151
Nellcor Covidien LP 138
Nonin Nonin Medical, Inc. 129
Orantech Orantech Inc. 97
Med-link Shenzhen MED-Link Electronics Tech Co., Ltd. 93
Welch Allyn, Inc. Welch Allyn, Inc. 66
Medichoice Owens & Minor Distribution, Inc. 62
Caremed Shenzhen Caremed Medical Technology Co., Ltd. 55
Sensoronics Sensoronics Incorporated 53
Virtuox Healthcare Logistics Systems 36

Showing 12 of 1,063. All products under Oximeter

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K082888 2008-11-26
K061329 2006-07-07
K032537 2003-11-25

Recalls Naming This Product

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

Recalls naming the identifiers of Infinity Mcable-Nellcor Oximax
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Draeger Medical Systems, Inc. 510(k) number 2020-12-23 Class II Software design The Infinity M540 patient monitor may randomly reboot due to an error to correctly transmit and read the header data of files in the memory of the device. Under this situation, the device will try to reboot to mitigate the error. The device 19802 systems (Domestic: 3412, Foreign 16,390)
Draeger Medical Systems, Inc. 510(k) number 2019-09-13 Class II Software design Cybersecurity vulnerabilities may cause device to reboot, lose alarm functionality, and/or lose communication with cockpit and/or the Infinity Network. 5634
Draeger Medical Systems, Inc. 510(k) number 2018-03-28 Class II Under Investigation by firm Software anomaly resulting in the loss of patient settings and stored patient data. 25, 629 2020-04-21
Draeger Medical Systems, Inc. 510(k) number 2018-02-21 Class II Software Manufacturing/Software Deployment The invasive pressure visual and audible alarms may not activate. 28317 total products 2020-04-20
Draeger Medical Systems, Inc. 510(k) number 2017-10-04 Class II Nonconforming Material/Component Dual Hemo MCable Pods with Revision
Index (RI) 15 and 16, which are used with the Drger Infinity Acute Care System, may
permit liquid ingress inconsistent with their IPX4 rating, which could potentially result in an
incorrect measured value
2,760 2018-06-15
Draeger Medical Systems, Inc. 510(k) number 2017-06-06 Class II Software design Cockpits with revision index 06 or higher that contain 4GB RAM modules may not annunciate audio or visual alarms on the Cockpit and Central Station. 37 US and 682 OUS 2018-06-19
Draeger Medical Systems, Inc. 510(k) number 2013-12-10 Class II Software design After a test in which a low SpO2 (yellow) medium grade alarm initiated in neo-natal mode and was subsequently paused, the high grade life threatening SpO2 alarm (red) did not activate when the SpO2 values were decreased to reach the red ala 439 2015-05-20
Draeger, Inc. 510(k) number 2012-12-13 Class II Labeling design The displayed value for the invasive blood pressure measurement of the IACS was different than the actual patient values. Liquid ingress in the cable connection may cause inaccurate measurements. This can happen if the Dual Hemo MCable is 260 2013-05-20

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