Hako-Med

GUDID 04260653010023

HAKO-MED Herstellung + Vertrieb von medizinisch-technischen Geräten G.m.b.H.

Interferential electrical stimulation system
Primary Device ID04260653010023
NIH Device Record Keyfae7cf6e-a39d-40c8-bf97-065468478f5a
Commercial Distribution StatusIn Commercial Distribution
Brand NameHako-Med
Version Model NumberElecDT
Company DUNS331405535
Company NameHAKO-MED Herstellung + Vertrieb von medizinisch-technischen Geräten G.m.b.H.
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 Batchfalse
Serial Numbertrue
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
GS104260653010023 [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 Date2019-11-18
Device Publish Date2019-11-08

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