Myo Plus trial kit

GUDID 04032767946761

Otto Bock Healthcare Products GmbH

Myoelectric hand prosthesis

• Primary Device ID: 04032767946761
• NIH Device Record Key: 6ac6dcc9-d91d-4a43-a99e-536e4c3e27dd
• Commercial Distribution Discontinuation: 2020-03-18
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Myo Plus trial kit
• Version Model Number: 642V64=T-PLUS-OB
• Company DUNS: 300802068
• Company Name: Otto Bock Healthcare Products 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: true
• 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	04032767946761 [Primary]

FDA Product Code

• GXY: Electrode, Cutaneous

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2020-03-20
• Device Publish Date: 2019-09-10

On-Brand Devices [Myo Plus trial kit]

• 04032767949199: 642V64=T-PLUS-S
• 04032767946761: 642V64=T-PLUS-OB
• 04064411245357: 642V64=T-PLUS-S
• 04064411245340: 642V64=T-PLUS-OB