Touch CMC 1 - Kirschner wire

GUDID 07640181163335

Keri Medical SA

Orthopaedic surgical procedure kit, non-medicated, reusable

• Primary Device ID: 07640181163335
• NIH Device Record Key: 049c8acd-e7e5-4621-8788-923011a4dafb
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Touch CMC 1 - Kirschner wire
• Version Model Number: 000-A00650
• Company DUNS: 480138827
• Company Name: Keri Medical SA
• Device Count: 10
• DM Exempt: true
• 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: true
• Expiration Date: false
• 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	07640181163106 [Primary]
GS1	07640181163335 [Unit of Use]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Approval: P240020

FDA Product Code

• HXI: Passer, Wire, Orthopedic
• SFA: Prosthesis, Finger, Semi-Constrained, Metal/Polymer

Sterilization

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

[07640181163335]

Moist Heat or Steam Sterilization

[07640181163335]

Moist Heat or Steam Sterilization

[07640181163335]

Moist Heat or Steam Sterilization

[07640181163335]

Moist Heat or Steam Sterilization

[07640181163335]

Moist Heat or Steam Sterilization

[07640181163335]

Moist Heat or Steam Sterilization

[07640181163335]

Moist Heat or Steam Sterilization

[07640181163335]

Moist Heat or Steam Sterilization

[07640181163335]

Moist Heat or Steam Sterilization

[07640181163335]

Moist Heat or Steam Sterilization

[07640181163335]

Moist Heat or Steam Sterilization

[07640181163335]

Moist Heat or Steam Sterilization

[07640181163335]

Moist Heat or Steam Sterilization

[07640181163335]

Moist Heat or Steam Sterilization

[07640181163335]

Moist Heat or Steam Sterilization

[07640181163335]

Moist Heat or Steam Sterilization

[07640181163335]

Moist Heat or Steam Sterilization

[07640181163335]

Moist Heat or Steam Sterilization

[07640181163335]

Moist Heat or Steam Sterilization

[07640181163335]

Moist Heat or Steam Sterilization

[07640181163335]

Moist Heat or Steam Sterilization

[07640181163335]

Moist Heat or Steam Sterilization

[07640181163335]

Moist Heat or Steam Sterilization

[07640181163335]

Moist Heat or Steam Sterilization

[07640181163335]

Moist Heat or Steam Sterilization

[07640181163335]

Moist Heat or Steam Sterilization

[07640181163335]

Moist Heat or Steam Sterilization

[07640181163335]

Moist Heat or Steam Sterilization

[07640181163335]

Moist Heat or Steam Sterilization

[07640181163335]

Moist Heat or Steam Sterilization

[07640181163335]

Moist Heat or Steam Sterilization

[07640181163335]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-07-29
• Device Publish Date: 2025-07-21

Devices Manufactured by Keri Medical SA

• 07640181161256 - Forked retractor: 2026-03-17
• 07640181160945 - Metacarpal rasp 0: 2026-03-10
• 07640181160952 - Metacarpal rasp 1: 2026-03-10
• 07640181160969 - Metacarpal rasp 2: 2026-03-10
• 07640181160976 - Metacarpal rasp 3: 2026-03-10
• 07640181160983 - Metacarpal rasp 4: 2026-03-10
• 07640181160990 - Metacarpal rasp XS: 2026-03-10
• 07640181160808 - Touch CMC 1 - Straight Neck Pattern 6-S: 2025-07-29