Lamination pattern for outer socket

GUDID 04032767159970

Otto Bock Healthcare Products GmbH

Myoelectric hand prosthesis

• Primary Device ID: 04032767159970
• NIH Device Record Key: f11ad6e0-6551-44e0-9a5a-e791ac309a8e
• Commercial Distribution Discontinuation: 2020-03-18
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Lamination pattern for outer socket
• Version Model Number: 13E192
• 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: false
• 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	04032767159970 [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: 3
• Public Version Date: 2020-03-19
• Device Publish Date: 2016-09-23

On-Brand Devices [Lamination pattern for outer socket]

• 04032767253913: 13E204
• 04032767159970: 13E192