advansor-tf

GUDID 00857356008309

Trigger Finger Release System

TRICE MEDICAL, INC.

Orthopaedic surgical procedure kit, non-medicated, single-use Orthopaedic surgical procedure kit, non-medicated, single-use Orthopaedic surgical procedure kit, non-medicated, single-use Orthopaedic surgical procedure kit, non-medicated, single-use Orthopaedic surgical procedure kit, non-medicated, single-use Orthopaedic surgical procedure kit, non-medicated, single-use Orthopaedic surgical procedure kit, non-medicated, single-use Orthopaedic surgical procedure kit, non-medicated, single-use Orthopaedic surgical procedure kit, non-medicated, single-use Orthopaedic surgical procedure kit, non-medicated, single-use Orthopaedic surgical procedure kit, non-medicated, single-use Orthopaedic surgical procedure kit, non-medicated, single-use Orthopaedic surgical procedure kit, non-medicated, single-use Orthopaedic surgical procedure kit, non-medicated, single-use Orthopaedic surgical procedure kit, non-medicated, single-use Orthopaedic surgical procedure kit, non-medicated, single-use Orthopaedic surgical procedure kit, non-medicated, single-use Orthopaedic surgical procedure kit, non-medicated, single-use

• Primary Device ID: 00857356008309
• NIH Device Record Key: ea965e98-62f1-4c7b-9655-471df51a7b54
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: advansor-tf
• Version Model Number: T500-010
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00857356008309 [Primary]
GS1	00857356008712 [Package]; Package: [10 Units]; In Commercial Distribution

FDA Product Code

• KDD: Kit, Surgical Instrument, Disposable

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: 2023-03-10
• Device Publish Date: 2023-03-02

Devices Manufactured by TRICE MEDICAL, INC.

• 00857356008026 - mi-eye 2: 2023-11-17 MI-EYE 2 SYSTEM, MI-ULTRA, EN
• 00857356008118 - mi-eye 2: 2023-11-17 TRICE MI-EYE ANGLED NEEDLESCOPE, 120MM
• 00857356008224 - mi-tablet 3: 2023-11-17 mi-tablet 3
• 00857356008231 - mi-eye 3: 2023-11-17 mi-eye 3 needlescope, 95mm
• 00857356008248 - mi-eye 3: 2023-11-17 mi-eye 3 angled scope, 120mm
• 00857356008255 - mi-eye 3: 2023-11-17 mi-eye 3 25 deg scope, 75mm with cannula
• 00857356008262 - mi-eye 3: 2023-11-17 mi-eye 3 scope, 95mm with cannula
• 00857356008279 - mi-eye 3: 2023-11-17 mi-eye 3 25° scope, 75mm with cannula