Life Scope L

Bedside Monitor

Registry build 21.09.26
9manufacturers in China registered for this device type
2catalogue numbers in this listing
6510(k) clearances naming this product 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 Life Scope L
Listed by Nihon Kohden Corp., Japan
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, Manufacturer
Record published 2017-01-05
Record revised 2024-03-04 (version 7)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Prescription Prescription only
Label carries serial number

Catalogue Numbers

Catalogue numbers for Life Scope L
Catalogue number Size Status
BSM-2351A In distribution
BSM-2354A In distribution

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
K203435 2021-07-16
K163459 2017-04-04
K153707 2016-09-02
K151080 2015-11-05
K112637 2011-12-09
K102376 2010-12-07

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