FDA Device Intelligence
HomeHASOMED GmbH › RehaStim 2 / RehaMove 2

RehaStim 2 / RehaMove 2

HASOMED GmbH · Model FES00005 · UDI-DI 04260397620168

GZI Prescription
1
510(k) clearances
50
Adverse events (1 deaths)
2
Recalls
41
Facilities

Description

powered muscle stimulator (8 channels) for use as stand-alone device as well as in combination with powered exerciser with predefined programs for stimulation of muscles of the musculoskeletal system

Recalls

DateFirmReason
2022-07-19Myolyn Inc.Screws mounting an internal power supply may come loose during shipping resulting in increased risk of high voltage electrical shock.
2008-08-06Innovative Neurotronics, Inc.Knob responsible for regulating the amount of stimulation administered by the WalkAide System control unit may fall off while device is in use.

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.