Insertion Tube STR-66IT01-00

GUDID 07290014954786

ALPHA OMEGA ENGINEERING CO. LTD.

Intracerebral cannula, implantable

• Primary Device ID: 07290014954786
• NIH Device Record Key: 0867a5f2-e854-4fb5-b05c-a94a87c1e8ab
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Insertion Tube
• Version Model Number: Set 40mm above
• Catalog Number: STR-66IT01-00
• 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 8779196288
• Email: m.andrea@alphaomega-eng.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	07290014954786 [Primary]
GS1	17290014954783 [Package]; Package: carton [10 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K120098

FDA Product Code

• GZL: Electrode, Depth

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2019-11-22
• Device Publish Date: 2016-09-24

Devices Manufactured by ALPHA OMEGA ENGINEERING CO. LTD.

• 07290114064057 - Remote Control: 2024-01-12
• 07290114064064 - Remote Control: 2024-01-12
• 07290114064071 - HaGuide Software: 2024-01-09
• 07290114064149 - Bengun W/O Screws: 2024-01-09
• 07290114064156 - Bengun Adapter: 2024-01-09
• 07290014954083 - NeuroSmart Main Unit: 2024-01-08
• 07290016450019 - NeuroSmart MER Headstage: 2024-01-08
• 07290114060790 - NeuroSmart NeuroForits Drive Headstage: 2024-01-08