SENSIMED Triggerfish® Sensor MEDIUM BO3M

GUDID 07640153470058

A box of three MEDIUM SENSIMED Triggerfish® Sensors

Sensimed SA

Ocular volume ambulatory recording system sensor

• Primary Device ID: 07640153470058
• NIH Device Record Key: 96f9808e-9ea6-4706-b50a-71378c30f3c1
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SENSIMED Triggerfish® Sensor MEDIUM
• Version Model Number: M.V.4
• Catalog Number: BO3M
• Company DUNS: 482491177
• Company Name: Sensimed SA
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Unsafe
• 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

Customer Support Contacts

• Phone: +41216219191
• Email: info@sensimed.ch

Device Identifiers

Device Issuing Agency	Device ID
GS1	07640153470058 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• deNovo: DEN140017

FDA Product Code

• PLZ: Ocular Pattern Recorder

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: 2017-06-20

On-Brand Devices [SENSIMED Triggerfish® Sensor MEDIUM]

• 07640153470058: A box of three MEDIUM SENSIMED Triggerfish® Sensors
• 07640153470027: A single unit of MEDIUM SENSIMED Triggerfish® Sensor