Myo Plus trial kit

GUDID 04064411245340

Otto Bock Healthcare Products GmbH

Myoelectric hand prosthesis

• Primary Device ID: 04064411245340
• NIH Device Record Key: 65d4e7f7-5e7b-4ec0-a22b-4bd3a7f583e1
• Commercial Distribution Status: 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: 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	04064411245340 [Primary]

FDA Product Code

• GXY: Electrode, Cutaneous

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: 2020-03-27
• Device Publish Date: 2020-03-19

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