Holter Monitor

Catalogue number Model 950-3CH, listed by Memtec Corporation, United States, under Recorder, Magnetic Tape, Medical. 4 manufacturers in China are registered for this product code.

Registry build 21.09.26
4manufacturers in China registered for this device type
1catalogue number
1510(k) clearance

Who Else Makes It

Concentrated in Guangdong (3), Jiangsu (1). One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code DSH
Manufacturer City Province Registered as Device types
Amphenol Medical Technologies (Dongguan) Co., Ltd. Dongguan Guangdong Contract manufacturer 77
Edan Instruments, Inc. Shenzhen Guangdong Contract manufacturer 56
Shenzhen Creative Industry Co., Ltd. Shenzhen Guangdong Manufacturer 9
Biox Instruments Co Ltd Wuxi Jiangsu Manufacturer 2

Record

Regulatory record for Holter Monitor
Listed by Memtec Corporation, United States
FDA product code DSH
Device type Recorder, Magnetic Tape, Medical
Device class Class 2
Regulation 21 CFR 870.2800
Record published 2019-11-15

Specifications

Specifications
MRI safety MR Unsafe
Single use Yes
Prescription Prescription only
Supplied as a kit Yes
Distribution end date 2029-11-15
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for Holter Monitor
Catalogue number Size Status
Model 950-3CH In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Spacelabs Healthcare Spacelabs Healthcare (Washington), Inc 33
Matrix Wearable Global Instrumentation, LLC 12
CardioSTAT Icentia Inc 6
Holter ECG and ABP System Edan Instruments, Inc. 5
Epatch Sensor Braemar Manufacturing, LLC 5
Welch Allyn, Inc. Welch Allyn, Inc. 4
Nuubo System Smart Solutions Technologies SL 4
VitaloJAK Vitalograph Ireland Ltd. 4
Care Assist Philips Medizin Systeme Böblingen GmbH 4
AT-Patch ATsens Co., Ltd. 3
Cuff ABPMpro without ECG Somnomedics AG 3
Vasomedical-Biox™ Arcs S/W Dongle – Mini 1200/1201 2 & 3 CH ECG Vasomedical, Inc. 3

Showing 12 of 122. All products under Recorder, Magnetic Tape, Medical

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K944180 1997-03-07

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