DYNOSENSE

GUDID 06953825902438

Shenzhen Urion Technology Co., Ltd

Automatic-inflation electronic sphygmomanometer, portable, arm/wrist Automatic-inflation electronic sphygmomanometer, portable, arm/wrist Automatic-inflation electronic sphygmomanometer, portable, arm/wrist Automatic-inflation electronic sphygmomanometer, portable, arm/wrist Automatic-inflation electronic sphygmomanometer, portable, arm/wrist Automatic-inflation electronic sphygmomanometer, portable, arm/wrist Automatic-inflation electronic sphygmomanometer, portable, arm/wrist Automatic-inflation electronic sphygmomanometer, portable, arm/wrist Automatic-inflation electronic sphygmomanometer, portable, arm/wrist Automatic-inflation electronic sphygmomanometer, portable, arm/wrist Automatic-inflation electronic sphygmomanometer, portable, arm/wrist Automatic-inflation electronic sphygmomanometer, portable, arm/wrist Automatic-inflation electronic sphygmomanometer, portable, arm/wrist Automatic-inflation electronic sphygmomanometer, portable, arm/wrist Automatic-inflation electronic sphygmomanometer, portable, arm/wrist Automatic-inflation electronic sphygmomanometer, portable, arm/wrist
Primary Device ID06953825902438
NIH Device Record Keyd076575e-4a76-4d75-bae4-5bd8a494a0c5
Commercial Distribution StatusIn Commercial Distribution
Brand NameDYNOSENSE
Version Model NumberU60AH
Company DUNS421294358
Company NameShenzhen Urion Technology Co., Ltd
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numbertrue
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS106953825902438 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

DXNSystem, Measurement, Blood-Pressure, Non-Invasive

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number6
Public Version Date2020-04-09
Device Publish Date2016-12-28

Devices Manufactured by Shenzhen Urion Technology Co., Ltd

16953825907706 - N/A2023-12-04
16953825907669 - WUJIE2023-11-22
16953825907676 - SDUNW2023-11-16
16953825907553 - N/A2023-09-25
16953825907539 - Baseline Evaluation Instruments2023-09-21
16953825907522 - Baseline Evaluation Instruments2023-09-14
16953825907478 - Rgdood2023-09-11
16953825907492 - MEDCURSOR2023-09-11

Trademark Results [DYNOSENSE]

Mark Image

Registration | Serial
Company
Trademark
Application Date
DYNOSENSE
DYNOSENSE
86603884 5138155 Live/Registered
DynoSense Corp.
2015-04-21

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.