RENPHO Eye Massager

GUDID 10810140060423

Joicom Corporation

Hand-held electric massager Hand-held electric massager Hand-held electric massager Hand-held electric massager Hand-held electric massager Hand-held electric massager Hand-held electric massager Hand-held electric massager Hand-held electric massager Hand-held electric massager Hand-held electric massager Hand-held electric massager Hand-held electric massager Hand-held electric massager Hand-held electric massager Hand-held electric massager Hand-held electric massager
Primary Device ID10810140060423
NIH Device Record Keye210b2f1-48e4-4687-a6bf-aaa2c48ddf9d
Commercial Distribution StatusIn Commercial Distribution
Brand NameRENPHO Eye Massager
Version Model NumberRF-EM001R
Company DUNS033774836
Company NameJoicom Corporation
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
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
GS100810140060426 [Primary]
GS110810140060423 [Package]
Contains: 00810140060426
Package: case [12 Units]
In Commercial Distribution
GS120810140060420 [Package]
Contains: 00810140060426
Package: case [12 Units]
In Commercial Distribution

FDA Product Code

ISAMassager, Therapeutic, Electric

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-08-15
Device Publish Date2023-08-07

On-Brand Devices [RENPHO Eye Massager]

10810140060423RF-EM001R
10810140060416RF-EM001R
10810140060409RF-EM001
10810140060362RF-EM001
10810140060355RF-EM001

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