GUDID 04582275270044

KONAN MEDICAL USA, INC.

Visual evoked-potential electrode

• Primary Device ID: 04582275270044
• NIH Device Record Key: e2a0f77a-6802-427e-8c81-c41ffa97ff61
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: M379 DME CARBON R
• Company DUNS: 788439219
• Company Name: KONAN MEDICAL USA, INC.
• 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: true
• 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	04582275270044 [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: 2018-03-29
• Device Publish Date: 2016-09-23

Devices Manufactured by KONAN MEDICAL USA, INC.

• 04582275270075 - NA: 2024-08-12
• 04582275270068 - NA: 2023-06-23
• 04582275270051 - N/A: 2019-09-17
• 04582275270020 - NA: 2018-07-06
• 04582275270037 - NA: 2018-03-29
• 04582275270044 - NA: 2018-03-29
• 04582275270044 - NA: 2018-03-29