RENPHO Eye Massager

GUDID 00810140061775

Joicom Corporation

Hand-held electric massager
Primary Device ID00810140061775
NIH Device Record Key4073e4df-5f62-4e02-863e-eb08501033d4
Commercial Distribution StatusIn Commercial Distribution
Brand NameRENPHO Eye Massager
Version Model NumberR-WME01
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
GS100810140061775 [Primary]
GS110810140061772 [Package]
Package: case [16 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 Date2025-06-06
Device Publish Date2025-05-29

On-Brand Devices [RENPHO Eye Massager]

10810140061185R-G010V
10810140060492R-G006
10810140060485R-G006
10810140060478R-G006
10810140060461R-G004
10810140060447RF-EM001R
10810140060430RF-EM001R
10810140060393RF-EM001
10810140060386RF-EM001
10810140060379RF-EM001
00810140062499R-WME02
00810140062451R-G006
00810140062444R-WME04
00810140062437R-WME02
00810140061928RF-EM001V
00810140061911R-G010V
00810140061775R-WME01
00810140061713R-G010V
00810140061584R-G011
00810140061577RF-EM001V
00810140061508R-G006
00810140061492R-GC001
00810140061485R-G010V
00810140061263RF-EM001
00810140061249RF-EM001

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