MEP 4520

GUDID 08519520070087

EMG Sensor

PERSONAL MEDICAL CORP.

Perineometer
Primary Device ID08519520070087
NIH Device Record Key08f1d6fb-4714-4f71-886e-aaf48705f093
Commercial Distribution Discontinuation2025-12-31
Commercial Distribution StatusNot in Commercial Distribution
Brand NameMEP
Version Model NumberAnal Sensor
Catalog Number4520
Company DUNS078511333
Company NamePERSONAL MEDICAL CORP.
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 Numberfalse
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone425-242-6373
Emailinfo@personalmed.com
Phone425-242-6373
Emailinfo@personalmed.com
Phone425-242-6373
Emailinfo@personalmed.com
Phone425-242-6373
Emailinfo@personalmed.com
Phone425-242-6373
Emailinfo@personalmed.com
Phone425-242-6373
Emailinfo@personalmed.com
Phone425-242-6373
Emailinfo@personalmed.com

Device Identifiers

Device Issuing AgencyDevice ID
GS108519520070087 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

HIRPerineometer

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2025-12-31
Device Publish Date2016-12-06

On-Brand Devices [MEP]

08519520070087EMG Sensor
08519520070010EMG Sensor

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