Flex-MI

GUDID 00859718007272

Emsi

Physical therapy transcutaneous neuromuscular electrical stimulation system Physical therapy transcutaneous neuromuscular electrical stimulation system Physical therapy transcutaneous neuromuscular electrical stimulation system Physical therapy transcutaneous neuromuscular electrical stimulation system Physical therapy transcutaneous neuromuscular electrical stimulation system Physical therapy transcutaneous neuromuscular electrical stimulation system Physical therapy transcutaneous neuromuscular electrical stimulation system Physical therapy transcutaneous neuromuscular electrical stimulation system Physical therapy transcutaneous neuromuscular electrical stimulation system Physical therapy transcutaneous neuromuscular electrical stimulation system Physical therapy transcutaneous neuromuscular electrical stimulation system Physical therapy transcutaneous neuromuscular electrical stimulation system Physical therapy transcutaneous neuromuscular electrical stimulation system Physical therapy transcutaneous neuromuscular electrical stimulation system Physical therapy transcutaneous neuromuscular electrical stimulation system Physical therapy transcutaneous neuromuscular electrical stimulation system Physical therapy transcutaneous neuromuscular electrical stimulation system
Primary Device ID00859718007272
NIH Device Record Keye24a5e48-fefd-46fa-a31e-8c91e03bb93e
Commercial Distribution StatusIn Commercial Distribution
Brand NameFlex-MI
Version Model NumberFLEMC0001
Company DUNS932471881
Company NameEmsi
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 Usetrue
Lot Batchfalse
Serial Numbertrue
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100859718007272 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

IPFStimulator, Muscle, Powered

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-09-27
Device Publish Date2023-09-19

Devices Manufactured by Emsi

00858688006964 - Electrode 45 x 45 16 PK2023-09-28
00858688006971 - Electrode 1.75 x 1.75 4 pack 2023-09-28
00859718007074 - Electrode 1.75 x 1.75 - 24 PK2023-09-28
00859718007081 - Electrode 4.0 x 7.0- Dispersive2023-09-28
00859718007098 - Electrode 1 Inch Round 4 PK2023-09-28
00859718007104 - Electrode 2" round 4pk2023-09-28
00859718007111 - Electrode 3 Inch Round 4PK2023-09-28
00859718007135 - Electrode 2 x 4 Inch Rectangle 2023-09-28

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