RehaStim 2 FES01050

GUDID 04260397620670

External Functional Neuromuscular Stimulator (8 channels), designed for use as stand-alone device as well as in combination with exercise equipment fo

HASOMED GmbH

Gait-enhancement electrical stimulation system, external

• Primary Device ID: 04260397620670
• NIH Device Record Key: 37dbec03-1adb-43c0-9dbb-4a1fed8578a5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: RehaStim 2
• Version Model Number: FES01050
• Catalog Number: FES01050
• Company DUNS: 341439008
• Company Name: HASOMED GmbH
• 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	04260397620670 [Primary]

FDA Product Code

• GZI: Stimulator, Neuromuscular, External Functional

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: 2018-07-06
• Device Publish Date: 2018-06-05

On-Brand Devices [RehaStim 2]

• 04260397620670: External Functional Neuromuscular Stimulator (8 channels), designed for use as stand-alone devic
• 04260397620342: External Functional Neuromuscular Stimulator (8 channels), designed for use as stand-alone devic