PulsioFlex

Catalogue number PC4000, listed by Pulsion Medical Systems SE, Germany, under Computer, Diagnostic, Pre-Programmed, Single-Function. 5 manufacturers in China are registered for this product code.

Registry build 21.09.26
5manufacturers in China registered for this device type
1catalogue number
3510(k) clearances naming this product code

Who Else Makes It

Concentrated in Guangdong (4), Jiangsu (1). One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code DXG
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
Orantech Inc. Shenzhen Guangdong Contract manufacturer 40
Shenzhen Comen Medical Instruments Co., Ltd. Shenzhen Guangdong Contract manufacturer 24

Record

Regulatory record for PulsioFlex
Listed by Pulsion Medical Systems SE, Germany
FDA product code DXG
Device type Computer, Diagnostic, Pre-Programmed, Single-Function
Device class Class 2
Regulation 21 CFR 870.1435
Establishment Contract manufacturer, Manufacturer
Record published 2017-03-10
Record revised 2026-06-29 (version 6)

Specifications

Specifications
MRI safety MR Unsafe
Label carries manufacturing date, serial number

Catalogue Numbers

Catalogue numbers for PulsioFlex
Catalogue number Size Status
PC4000 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
LiDCO Ltd Lidco Ltd. 133
LiDCO Lidco Ltd. 32
Transonic Transonic Systems, Inc. 31
Computer, Diagnostic, Pre-Programmed, Single-Function Edwards Lifesciences Technology Sarl 23
Retia Medical Retia Medical, LLC 17
EV1000 Edwards Lifesciences Technology Sarl 11
Computer, Diagnostic, Pre-Programmed, Single-Function GE Healthcare Finland OY 5
Pediasat Edwards Lifesciences Technology Sarl 4
LiDCO Masimo Corporation 4
ICU Medical ICU Medical, Inc 4
Cnap® Monitor 500 HD Cnsystems Medizintechnik GmbH 4
Vigileo Edwards Lifesciences Technology Sarl 3

Showing 12 of 39. All products under Computer, Diagnostic, Pre-Programmed, Single-Function

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K192169 2020-04-30
K172259 2018-01-18
K122121 2012-08-02

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