UltraviewSL

Option, Masimo SPO2, Refurbished

Registry build 21.09.26
98manufacturers in China registered for this device type
1catalogue number

Who Else Makes It

Concentrated in Guangdong (67), Jiangsu (11), Zhejiang (6). 17 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code DXN
Manufacturer City Province Registered as Device types
Amphenol Medical Technologies (Dongguan) Co., Ltd. Dongguan Guangdong Contract manufacturer 77
Andon Health Co., Ltd. Tianjin Tianjin Contract manufacturer 22
Taizhou Rich Medical Products Co., Ltd. Taizhou Jiangsu Contract manufacturer 20
Medwell Technology Limited Dongguan Guangdong Contract manufacturer 10
Honsun (Nantong) Co., Ltd. Nantong Jiangsu Contract manufacturer 9
EMI (Dongguan) Asia Limited Dongguan Guangdong Contract manufacturer 9
Yahorng Dongguan Electronic Co Ltd Guangdong Guangdong Contract manufacturer 8
Guangzhou Daxin Health Technology (Dongguan) Co., Ltd. Dongguan Guangdong Contract manufacturer 7
Omron (Dalian) Co., Ltd. (Plant 1) Dalian Liaoning Contract manufacturer 7
Wuhan Strong Electronics Wuhan Hubei Contract manufacturer 6
Dongguan Polygreen Technology Co., Ltd. Dongguan Guangdong Contract manufacturer 4
Shenzhen Brav Electronic Technologies Co., Ltd. Shenzhen Guangdong Contract manufacturer 3

Showing 12 of 98. All 98 manufacturers in China registered for System, Measurement, Blood-Pressure, Non-Invasive

Record

Regulatory record for UltraviewSL
Listed by Spacelabs Healthcare (Washington), Inc
FDA product code DXN
Device type System, Measurement, Blood-Pressure, Non-Invasive
Device class Class 2
Regulation 21 CFR 870.1130
510(k) K103142
Record published 2016-11-15
Record revised 2024-05-08 (version 5)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Prescription Prescription only
Label carries serial number
Storage Storage environment temperature -40 to 75 °C; Storage environment humidity 0 to 95 % RH
Distribution end date 2023-05-26

Catalogue Numbers

Catalogue numbers for UltraviewSL
Catalogue number Size Status
91496 Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Baum W.A. Baum Co., Inc. 116
Alphamed Shenzhen Urion Technology Co., Ltd. 68
Electronic Blood Pressure Monitor Shenzhen Pango Electronic Co., Ltd. 59
Arm Type Automatic Blood Pressure Monitor Shenzhen Jiacom Technology Co., Ltd. 58
A&D Medical A&D Company, Ltd. 56
Diagnostix™ American Diagnostic Corp. 54
Lutech Lutech Industries 51
Veridian Veridian Healthcare 50
Hopkins Medical Products® Hopkins Uniform Company 49
Welch Allyn, Inc. Welch Allyn, Inc. 49
Merit Medical® Argon Critical Care Systems Singapore PTE. Ltd. 48
SunTech Suntech Medical, Inc. 46

Showing 12 of 1,292. All products under System, Measurement, Blood-Pressure, Non-Invasive

Recalls Naming This Product

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

Recalls naming the identifiers of UltraviewSL
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Spacelabs Healthcare Ltd. 510(k) number 2026-03-26 Class II Process control Due to a manufacturing issue (i.e. malfunctioning of electrical Leakage tester). 57
Spacelabs Healthcare Ltd. 510(k) number 2026-02-27 Class II Component change control Multi-parameter command module has a circuit board issue and when in Auto mode, Cardiac Output (CO) measurement may activate early, resulting in Bad Curve error with no CO measurement or Irregular Curve error with CO measurement not automat 1790
Spacelabs Healthcare Ltd. 510(k) number 2023-04-12 Class II Component change control Command modules will display the following when parameter processing is suspended, depending on software version: 1) Older versions will have waveforms present with no alarms, 2) Newer versions have waveforms absent with no alarms. This may 1,088
Spacelabs Healthcare Ltd. 510(k) number 2016-07-01 Class II Vendor change control The firm has received multiple reports of the Non-Invasive Blood Pressure (NIBP) parameter becoming non-functional with an associated message (No Reading). In addition, there is one of the following three error messages: Inflate Error, HW E 3801 modules and 116 PCBAs & valves distributed in the US; 1 2017-05-22
Spacelabs Healthcare Ltd. 510(k) number 2015-04-21 Class II Software design Modules resetting. This failure mode happens when the Spacelabs Command Module is configured with the Masimo SpO2 option (-M), the Spacelabs Respiration option (-R) and the Masimo SpO2 PCBA, PN: 010-1136-02. With these two options and the M 1973 units total (1345 modules in the US and 604modules inte 2015-11-16
Spacelabs Healthcare Ltd. 510(k) number 2015-04-17 Class II Software design Ultraview SL Command Modules which were upgraded with the Masimo SpO2 Option, Model 91496-M was affected. Customer reported that during the time that the module is resetting (~10 seconds), monitoring of all parameters will be suspended. Up 1999 units total (1932 in the US and 67 international) 2015-11-13
Spacelabs Healthcare Ltd. 510(k) number 2014-05-08 Class II Software Manufacturing/Software Deployment A software anomaly causes temperature alarm limits to change to limits which are not physiologically possible and result in nuisance false positive alarms. 64 devices 2014-06-03
Spacelabs Healthcare Ltd. 510(k) number 2011-11-03 Not classified Process change control NIBP pump inside the Ultraview SL Command Module, Model 91496, became loose. The pump is suspended by the air hoses and electrical connections, but there can be enough movement to
damage internal components and cause the module to fail.
6722 units worldwide (3598 units in US and 3124 units outsid 2012-09-19
Spacelabs Healthcare Ltd. 510(k) number 2011-07-13 Not classified Software design One Spacelabs Medical Ultraview SL Command Module, Model 91496, was removed from customer due to software error. one unit 2012-01-20

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