DP-50T Digital Ultrasonic Diagnostic Imaging System

GUDID 06936415978136

Shenzhen Mindray Bio-Medical Electronics Co., Ltd.

General-purpose ultrasound imaging system
Primary Device ID06936415978136
NIH Device Record Key89c98efe-4594-40f7-8e85-3ec0ff3c6a07
Commercial Distribution StatusIn Commercial Distribution
Brand NameDP-50T Digital Ultrasonic Diagnostic Imaging System
Version Model NumberDP-50T
Company DUNS654671304
Company NameShenzhen Mindray Bio-Medical Electronics Co., Ltd.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Unsafe
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numbertrue
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS106936415978136 [Primary]

FDA Product Code

IYOSystem, Imaging, Pulsed Echo, Ultrasonic

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2025-01-30
Device Publish Date2025-01-22

Devices Manufactured by Shenzhen Mindray Bio-Medical Electronics Co., Ltd.

06903053000451 - BeneVision N17 Neo Patient Monitor2025-02-03
06903053000468 - BeneVision N15 Neo Patient Monitor2025-02-03
06903053037747 - BeneVision M17C Patient Monitor2025-02-03
06903053037754 - BeneVision M15C Patient Monitor2025-02-03
06903053037761 - BeneVision M12C Patient Monitor2025-02-03
06903053037778 - BeneVision M19C Patient Monitor2025-02-03
06903053037785 - BeneVision M22C Patient Monitor2025-02-03
06903053064453 - BeneVision N22 OR Patient Monitor2025-02-03

© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.