ACS-715

GUDID 03664539000824

WRENCH FOR ANCHOR BOLT REMOVAL, ACCESSORY OF MICRODEEP DEPTH ELECTRODE

DIXI MEDICAL

Depth electrode

• Primary Device ID: 03664539000824
• NIH Device Record Key: 4035abe1-aceb-4f63-af01-f15c94ffb8ed
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: WRENCH
• Catalog Number: ACS-715
• Company DUNS: 268009609
• Company Name: DIXI MEDICAL
• 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: true
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +33381889890
• Email: info@diximedical.com
• Phone: +33381889890
• Email: info@diximedical.com
• Phone: +33381889890
• Email: info@diximedical.com
• Phone: +33381889890
• Email: info@diximedical.com
• Phone: +33381889890
• Email: info@diximedical.com
• Phone: +33381889890
• Email: info@diximedical.com
• Phone: +33381889890
• Email: info@diximedical.com
• Phone: +33381889890
• Email: info@diximedical.com
• Phone: +33381889890
• Email: info@diximedical.com
• Phone: +33381889890
• Email: info@diximedical.com
• Phone: +33381889890
• Email: info@diximedical.com
• Phone: +33381889890
• Email: info@diximedical.com
• Phone: +33381889890
• Email: info@diximedical.com
• Phone: +33381889890
• Email: info@diximedical.com
• Phone: +33381889890
• Email: info@diximedical.com
• Phone: +33381889890
• Email: info@diximedical.com
• Phone: +33381889890
• Email: info@diximedical.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	03664539000824 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K170959

FDA Product Code

• GZL: Electrode, Depth

Sterilization

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

[03664539000824]

Moist Heat or Steam Sterilization

[03664539000824]

Moist Heat or Steam Sterilization

[03664539000824]

Moist Heat or Steam Sterilization

[03664539000824]

Moist Heat or Steam Sterilization

[03664539000824]

Moist Heat or Steam Sterilization

[03664539000824]

Moist Heat or Steam Sterilization

[03664539000824]

Moist Heat or Steam Sterilization

[03664539000824]

Moist Heat or Steam Sterilization

[03664539000824]

Moist Heat or Steam Sterilization

[03664539000824]

Moist Heat or Steam Sterilization

[03664539000824]

Moist Heat or Steam Sterilization

[03664539000824]

Moist Heat or Steam Sterilization

[03664539000824]

Moist Heat or Steam Sterilization

[03664539000824]

Moist Heat or Steam Sterilization

[03664539000824]

Moist Heat or Steam Sterilization

[03664539000824]

Moist Heat or Steam Sterilization

[03664539000824]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2019-09-23
• Device Publish Date: 2017-12-14

Devices Manufactured by DIXI MEDICAL

• 03664539004037 - NA: 2024-10-01 SUBDURAL ELECTRODE WITH CONNECTION CABLE, STRIP, 1x4 CONTACTS
• 03664539004044 - NA: 2024-10-01 SUBDURAL ELECTRODE WITH CONNECTION CABLE, STRIP, 1x6 CONTACTS
• 03664539004051 - NA: 2024-10-01 SUBDURAL ELECTRODE WITH CONNECTION CABLE, STRIP, 1x8 CONTACTS
• 03664539004068 - NA: 2024-10-01 SUBDURAL ELECTRODE WITH CONNECTION CABLE, GRID, 2x4 CONTACTS
• 03664539004075 - NA: 2024-10-01 SUBDURAL ELECTRODE WITH CONNECTION CABLE, GRID, 2x6 CONTACTS
• 03664539004082 - NA: 2024-10-01 SUBDURAL ELECTRODE WITH CONNECTION CABLE, GRID, 2x8 CONTACTS
• 03664539004099 - NA: 2024-10-01 SUBDURAL ELECTRODE WITH CONNECTION CABLE, GRID, 4x4 CONTACTS
• 03664539003900 - NA: 2024-04-11 GUIDE FOR Ø 2.45MM ACCESSORIES ACCESSORY OF MICRODEEP DEPTH ELECTRODE