V11-3Hs Ultrasonic Probe(FDA)

GUDID 06936415925925

Shenzhen Mindray Bio-Medical Electronics Co., Ltd.

Rectal/vaginal ultrasound imaging transducer
Primary Device ID06936415925925
NIH Device Record Key6bd76e86-9784-499c-8d42-d49fa1e425d3
Commercial Distribution StatusIn Commercial Distribution
Brand NameV11-3Hs Ultrasonic Probe(FDA)
Version Model Number120-018847-00
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

Customer Support Contacts

Phone+8675581888998
Emailservice@mindray.com.cn
Phone+8675581888998
Emailservice@mindray.com.cn
Phone+8675581888998
Emailservice@mindray.com.cn
Phone+8675581888998
Emailservice@mindray.com.cn
Phone+8675581888998
Emailservice@mindray.com.cn
Phone+8675581888998
Emailservice@mindray.com.cn
Phone+8675581888998
Emailservice@mindray.com.cn
Phone+8675581888998
Emailservice@mindray.com.cn
Phone+8675581888998
Emailservice@mindray.com.cn
Phone+8675581888998
Emailservice@mindray.com.cn
Phone+8675581888998
Emailservice@mindray.com.cn
Phone+8675581888998
Emailservice@mindray.com.cn
Phone+8675581888998
Emailservice@mindray.com.cn
Phone+8675581888998
Emailservice@mindray.com.cn

Device Identifiers

Device Issuing AgencyDevice ID
GS106936415925925 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

ITXTransducer, Ultrasonic, Diagnostic

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-12-07
Device Publish Date2020-11-29

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06903053039703 - P8-2s Transducer(FDA-SJM)2023-05-30

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