FEMTO LDV 510.003.002

GUDID 07640167750047

SIE AG, Surgical Instrument Engineering

Femtosecond ophthalmic solid-state laser system

• Primary Device ID: 07640167750047
• NIH Device Record Key: 2fce4bff-540d-4ef7-8e3c-24f2371ae352
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: FEMTO LDV
• Version Model Number: Z2
• Catalog Number: 510.003.002
• Company DUNS: 482163628
• Company Name: SIE AG, Surgical Instrument Engineering
• 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: false
• Lot Batch: false
• Serial Number: true
• Manufacturing Date: false
• 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

Customer Support Contacts

• Phone: 8667084490
• Email: usa@ziemergroup.com

Operating and Storage Conditions

• Storage Environment Temperature: Between 0 Degrees Celsius and 50 Degrees Celsius
• Storage Environment Humidity: Between 10 Percent (%) Relative Humidity and 80 Percent (%) Relative Humidity
• Storage Environment Atmospheric Pressure: Between 500 millibar and 1080 millibar

Device Identifiers

Device Issuing Agency	Device ID
GS1	07640167750047 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K112154

FDA Product Code

• HQF: Laser, Ophthalmic

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-09-15

On-Brand Devices [FEMTO LDV]

• 07640167750054: med-profile
• 07640167750047: Z2
• 07640167750030: Z4
• 07640167750023: Z6