TOUCH® CMC 1

GUDID 07640181160099

Keri Medical SA

Metacarpal prosthesis

• Primary Device ID: 07640181160099
• NIH Device Record Key: e630cb02-fd16-43ee-956c-06639a588351
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: TOUCH® CMC 1
• Version Model Number: CTO109
• Company DUNS: 480138827
• Company Name: Keri Medical SA
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Conditional
• 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: true
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	07640181160099 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Approval: P240020

FDA Product Code

• SFA: Prosthesis, Finger, Semi-Constrained, Metal/Polymer

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: 2025-07-28
• Device Publish Date: 2025-07-18

On-Brand Devices [TOUCH® CMC 1]

• 07640181160228: STOXS
• 07640181160150: STO4
• 07640181160143: STO3
• 07640181160136: STO2
• 07640181160129: STO1
• 07640181160112: STO0
• 07640181160105: CTO110
• 07640181160099: CTO109
• 07640181160082: CTO10
• 07640181160075: CTO09
• 07640181160068: NTO1510
• 07640181160051: NTO158
• 07640181160044: NTO156
• 07640181160037: NTO010
• 07640181160020: NTO08
• 07640181160013: NTO06