mi-eye Procedure Kit 5 pack

GUDID 10861578000376

pack of 5 T900-001

TRICE MEDICAL, INC.

Surgical patient preparation kit

• Primary Device ID: 10861578000376
• NIH Device Record Key: 1da195d8-4170-4c4d-bd27-2a2a29065923
• Commercial Distribution Discontinuation: 2025-02-28
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: mi-eye Procedure Kit 5 pack
• Version Model Number: T900-005
• 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: true
• 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: 610-989-8080
• Email: customercare@tricemedical.com
• Phone: 610-989-8080
• Email: customercare@tricemedical.com
• Phone: 610-989-8080
• Email: customercare@tricemedical.com
• Phone: 610-989-8080
• Email: customercare@tricemedical.com
• Phone: 610-989-8080
• Email: customercare@tricemedical.com
• Phone: 610-989-8080
• Email: customercare@tricemedical.com
• Phone: 610-989-8080
• Email: customercare@tricemedical.com
• Phone: 610-989-8080
• Email: customercare@tricemedical.com
• Phone: 610-989-8080
• Email: customercare@tricemedical.com
• Phone: 610-989-8080
• Email: customercare@tricemedical.com
• Phone: 610-989-8080
• Email: customercare@tricemedical.com
• Phone: 610-989-8080
• Email: customercare@tricemedical.com
• Phone: 610-989-8080
• Email: customercare@tricemedical.com
• Phone: 610-989-8080
• Email: customercare@tricemedical.com
• Phone: 610-989-8080
• Email: customercare@tricemedical.com
• Phone: 610-989-8080
• Email: customercare@tricemedical.com
• Phone: 610-989-8080
• Email: customercare@tricemedical.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	10861578000376 [Primary]

FDA Product Code

• KDD: Kit, Surgical Instrument, Disposable

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2025-03-03
• Device Publish Date: 2017-11-10

Devices Manufactured by TRICE MEDICAL, INC.

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• 00857356008781 - Tenex 2nd Generation MicroTip, TXS, 2.0 WL: 2025-03-14
• 00857356008798 - Tenex 2nd Generation MicroTip, TXS+, 1.3 WL: 2025-03-14
• 00857356008842 - Tenex 2nd Generation Console: 2025-03-14
• 00857356008859 - Tenex 2nd Generation Fuse Set: 2025-03-14
• 10861578000376 - mi-eye Procedure Kit 5 pack: 2025-03-03pack of 5 T900-001
• 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