Hako-Med

GUDID 04260653010023

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

Interferential electrical stimulation system Interferential electrical stimulation system Interferential electrical stimulation system Interferential electrical stimulation system Interferential electrical stimulation system Interferential electrical stimulation system Interferential electrical stimulation system Interferential electrical stimulation system Interferential electrical stimulation system Interferential electrical stimulation system Interferential electrical stimulation system Interferential electrical stimulation system Interferential electrical stimulation system Interferential electrical stimulation system Interferential electrical stimulation system

Primary Device ID	04260653010023
NIH Device Record Key	fae7cf6e-a39d-40c8-bf97-065468478f5a
Commercial Distribution Status	In Commercial Distribution
Brand Name	Hako-Med
Version Model Number	ElecDT
Company DUNS	331405535
Company Name	HAKO-MED Herstellung + Vertrieb von medizinisch-technischen Geräten G.m.b.H.
Device Count	1
DM Exempt	false
Pre-market Exempt	false
MRI Safety Status	Labeling does not contain MRI Safety Information
Human Cell/Tissue Product	false
Device Kit	false
Device Combination Product	false
Single Use	false
Lot Batch	false
Serial Number	true
Manufacturing Date	false
Expiration Date	false
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	false
RX Perscription	false
OTC Over-The-Counter	false

Device Identifiers

Device Issuing Agency	Device ID
GS1	04260653010023 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

Premarket Notification: K980892

FDA Product Code

IPF	Stimulator, Muscle, Powered

Sterilization

Steralize Prior To Use	false
Device Is Sterile	false

Device Entry Metadata

Public Version Status	New
Device Record Status	Published
Public Version Number	1
Public Version Date	2019-11-18
Device Publish Date	2019-11-08