Xhibit

KIT, Down Converter, Active Antenna

Registry build 21.09.26
10manufacturers in China registered for this device type
3catalogue numbers in this listing

Who Else Makes It

Concentrated in Guangdong (6), Jiangsu (1), Hebei (1). 2 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code DSI
Manufacturer City Province Registered as Device types
Amphenol Medical Technologies (Dongguan) Co., Ltd. Dongguan Guangdong Contract manufacturer 77
Linxens Healthcare (Tianjin) Co., Ltd. Jinnan District Tianjin Contract manufacturer 7
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
Orantech Inc. Shenzhen Guangdong Contract manufacturer 40
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
Shandong Corecare Technology Limited Jinan Shandong Manufacturer 2

Record

Regulatory record for Xhibit
Listed by Spacelabs Healthcare (Washington), Inc
FDA product code DSI
Device type Detector And Alarm, Arrhythmia
Device class Class 2
Regulation 21 CFR 870.1025
510(k) K141156
Record published 2018-08-10
Record revised 2023-10-05 (version 4)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Prescription Prescription only
Supplied as a kit Yes
Label carries lot or batch number, manufacturing date, serial number
Storage Storage environment temperature -40 to 75 °C
Distribution end date 2016-12-08

Catalogue Numbers

Catalogue numbers for Xhibit
Catalogue number Size Status
Xhibit Central In distribution
Xhibit Central In distribution
96102 Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Trulink Spacelabs Healthcare (Washington), Inc 160
Fukuda Denshi Fukuda Denshi Co., Ltd. 30
Q-Tel RMS Mortara Instrument, Inc. 20
Detector And Alarm, Arrhythmia Philips Medical Systems Hsg 20
ECG Electrodes Philips Medical Systems Hsg 19
Seeq™ Medtronic, Inc. 18
Life Sensing Instruments, Inc. Life Sensing Instruments, Inc. 17
NIBP Cuffs Philips Medical Systems Hsg 14
Waveline EZ+ Avante 11
BodyGuardian Preventice Technologies, Inc. 10
BodyGuardian Kit Preventice Technologies, Inc. 8
Waveline Pro+ Avante 7

Showing 12 of 112. All products under Detector And Alarm, Arrhythmia

Recalls Naming This Product

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

Recalls naming the identifiers of Xhibit
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Spacelabs Healthcare Ltd. 510(k) number 2026-06-04 Class II Unknown/Undetermined by firm Due to off-the-shelf display port component that has audio/video failures 6074
Spacelabs Healthcare Ltd. 510(k) number 2019-08-30 Class II Software Manufacturing/Software Deployment The firm received reports of loss of audio alarm after a power failure or cable disconnection. The loss of audio for a telemetry patient could delay the recognition of an alarm condition. 2197 units 2024-04-18
Spacelabs Healthcare Ltd. 510(k) number 2016-10-18 Class II Software design The firm received reports of telemetry SpO2 numerics dropping off the Xhibit Central display. Desaturation, high, and low limit alarms work normally. 348 units (292 units in the US and 56 units outside the US) 2017-04-03
Spacelabs Healthcare Ltd. 510(k) number 2016-08-25 Class II Software design The firm received multiple reports of Xhibit Telemetry System going offline or locking up. In addition, short-duration asystole alarms may not display an audio and visual alarm as reported from a single Canadian hospital. 798 units total (488 units in the US and 310 units outside U 2017-03-13
Spacelabs Healthcare Ltd. 510(k) number 2016-02-26 Class II Software in the Use Environment The firm has received one report of values for patient height and weight being switched when input at the Xhibit Central Station, Model 96102, causing a bedside monitor Body Surface Area (BSA) calculation to be in error. total 1075 units (614 units in the US and 461 outside the US 2016-10-24

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