pluse oximeter

GUDID 06951740540070

Shenzhen Jumper Medical Equipment Co.,Ltd.

Pulse oximeter
Primary Device ID06951740540070
NIH Device Record Key993565b4-ec5c-48c9-98cb-bf1c23a47a11
Commercial Distribution StatusIn Commercial Distribution
Brand Namepluse oximeter
Version Model NumberSPA30
Company DUNS529217911
Company NameShenzhen Jumper Medical Equipment 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
GS106951740540070 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

DQAOximeter

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-10-30
Device Publish Date2023-10-20

On-Brand Devices [pluse oximeter]

06951740540018pluse oximeter(white)
06951740538374pluse oximeter(white)
06951740538367pluse oximeter(black)
06951740500227JPD-500F
06951740500210JPD-500E
06951740500203JPD-500D
06951740500265JPD-500C
06951740500258JPD-500B
06951740500241JPD-500A
06951740540070SPA30
06951740540063SPA20
06951740540056SPA11
06951740540049SPA10

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