RENPHO Smart Blood Pressure Monitor

GUDID 30860002249699

JOICOM CORPORATION

Automatic-inflation electronic sphygmomanometer, portable, arm/wrist
Primary Device ID30860002249699
NIH Device Record Key6a836114-da91-4815-9d05-705bc3daeb0a
Commercial Distribution StatusIn Commercial Distribution
Brand NameRENPHO Smart Blood Pressure Monitor
Version Model NumberRP-BPM001S
Company DUNS081060692
Company NameJOICOM CORPORATION
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-Countertrue

Customer Support Contacts

Phone18444170149
Emailsupport@renpho.com
Phone18444170149
Emailsupport@renpho.com
Phone18444170149
Emailsupport@renpho.com
Phone18444170149
Emailsupport@renpho.com
Phone18444170149
Emailsupport@renpho.com
Phone18444170149
Emailsupport@renpho.com
Phone18444170149
Emailsupport@renpho.com
Phone18444170149
Emailsupport@renpho.com
Phone18444170149
Emailsupport@renpho.com
Phone18444170149
Emailsupport@renpho.com
Phone18444170149
Emailsupport@renpho.com
Phone18444170149
Emailsupport@renpho.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100860002249698 [Primary]
GS130860002249699 [Package]
Contains: 00860002249698
Package: Carton [40 Units]
In Commercial Distribution

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 StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-09-23
Device Publish Date2020-09-15

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