Digital Electrocardigraph

GUDID 06932562310072

Guangdong Biolight Meditech Co., Ltd.

Electrocardiograph, professional, multichannel
Primary Device ID06932562310072
NIH Device Record Key341d4572-446b-41c5-8acf-9739e1d01bf3
Commercial Distribution StatusIn Commercial Distribution
Brand NameDigital Electrocardigraph
Version Model NumberE70
Company DUNS530120146
Company NameGuangdong Biolight Meditech 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 Batchfalse
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
GS106932562310072 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

DPSElectrocardiograph

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2018-07-06
Device Publish Date2016-09-22

On-Brand Devices [Digital Electrocardigraph]

06932562310157E30
06932562310072E70

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