Neuro Omega MER Headstage KIT 750-020024-00

GUDID 27290114062453

ALPHA OMEGA ENGINEERING CO. LTD.

Depth electrode

• Primary Device ID: 27290114062453
• NIH Device Record Key: 4999afc3-0fe7-4246-be79-204503aa1c48
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Neuro Omega MER Headstage KIT
• Version Model Number: Neuro Omega MER Headstage KIT
• Catalog Number: 750-020024-00
• Company DUNS: 531856466
• Company Name: ALPHA OMEGA ENGINEERING CO. LTD.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Unsafe
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• 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	27290114062453 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K171581

FDA Product Code

• GZL: Electrode, Depth

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: 2023-06-26
• Device Publish Date: 2023-06-16

On-Brand Devices [Neuro Omega MER Headstage KIT]

• 27290016450167: Neuro Omega MER HeadStage KIT
• 27290114062453: Neuro Omega MER Headstage KIT