Icare tonometer probes

GUDID 06430033850565

ICARE FINLAND OY

Ophthalmic tonometer probe, sterile

• Primary Device ID: 06430033850565
• NIH Device Record Key: abcb24ee-8c10-42b8-893e-17f38d8df3b9
• Commercial Distribution Discontinuation: 2016-12-01
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Icare tonometer probes
• Version Model Number: TP01s
• Company DUNS: 651755092
• Company Name: ICARE FINLAND OY
• Device Count: 1
• DM Exempt: false
• 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• 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	06430033850565 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K063873

FDA Product Code

• HKX: Tonometer, Ac-Powered

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-12-01

Devices Manufactured by ICARE FINLAND OY

• 06430033851784 - ST500 SmartCradle: 2024-11-15 ST500 SmartCradle
• 06430033851791 - ST500 Adapter: 2024-11-15 ST500 Adapter
• 06430033851807 - ST500 Remote: 2024-11-15 ST500 Remote
• 06430033851883 - iCare ST500: 2024-11-15 iCare ST500 tonometer
• 06430033851098 - iCare PATIENT2: 2024-05-01 iCare PATIENT2 (iOS version)
• 06430033851104 - iCare PATIENT2: 2024-05-01 iCare PATIENT2 (Android version)
• 06430033851463 - iCare IC200: 2023-06-28 iCare IC200 (with Quick Measure feature)
• 06430033851456 - iCare HOME2: 2022-02-16