mi-probe T900-015

GUDID 00861578000393

mi-probe. surigcal instrument for soft tissue manipulation during mi-eye procedure

TRICE MEDICAL, INC.

Arthroscopic probe

• Primary Device ID: 00861578000393
• NIH Device Record Key: 1f4133f0-39a4-4a9e-b9bd-10c21fc58264
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: mi-probe
• Version Model Number: T900-011
• Catalog Number: T900-015
• Company DUNS: 009452895
• Company Name: TRICE MEDICAL, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: 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: 844.643.9300
• Email: customerservice@tricemedical.com
• Phone: 844.643.9300
• Email: customerservice@tricemedical.com
• Phone: 844.643.9300
• Email: customerservice@tricemedical.com
• Phone: 844.643.9300
• Email: customerservice@tricemedical.com
• Phone: 844.643.9300
• Email: customerservice@tricemedical.com
• Phone: 844.643.9300
• Email: customerservice@tricemedical.com
• Phone: 844.643.9300
• Email: customerservice@tricemedical.com
• Phone: 844.643.9300
• Email: customerservice@tricemedical.com
• Phone: 844.643.9300
• Email: customerservice@tricemedical.com
• Phone: 844.643.9300
• Email: customerservice@tricemedical.com
• Phone: 844.643.9300
• Email: customerservice@tricemedical.com
• Phone: 844.643.9300
• Email: customerservice@tricemedical.com
• Phone: 844.643.9300
• Email: customerservice@tricemedical.com
• Phone: 844.643.9300
• Email: customerservice@tricemedical.com
• Phone: 844.643.9300
• Email: customerservice@tricemedical.com
• Phone: 844.643.9300
• Email: customerservice@tricemedical.com
• Phone: 844.643.9300
• Email: customerservice@tricemedical.com
• Phone: 844.643.9300
• Email: customerservice@tricemedical.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00861578000386 [Primary]
GS1	00861578000393 [Package]; Contains: 00861578000386; Package: box [5 Units]; In Commercial Distribution

FDA Product Code

• HXB: Probe

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2018-05-11
• Device Publish Date: 2018-04-10

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• 00857356008842 - Tenex 2nd Generation Console: 2025-03-14
• 00857356008859 - Tenex 2nd Generation Fuse Set: 2025-03-14
• 10861578000376 - mi-eye Procedure Kit 5 pack: 2025-03-03 pack of 5 T900-001
• 00857356008026 - mi-eye 2: 2023-11-17 MI-EYE 2 SYSTEM, MI-ULTRA, EN