Treatment Pack (Size S)

GUDID 04049471110043

Single use patient interface for the VisuMax laser keratome

Carl Zeiss Meditec AG

Femtosecond ophthalmic solid-state laser system

• Primary Device ID: 04049471110043
• NIH Device Record Key: f3b7ba35-b070-4163-9c6a-fae286f59608
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Treatment Pack (Size S)
• Version Model Number: 1462-332
• Company DUNS: 314594680
• Company Name: Carl Zeiss Meditec AG
• Device Count: 10
• 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: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Dimensions

• Weight: 400 Gram
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	04049471100044 [Unit of Use]
GS1	04049471110043 [Primary]

FDA Product Code

• HQF: Laser, Ophthalmic

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2018-11-23
• Device Publish Date: 2016-09-23

On-Brand Devices [Treatment Pack (Size S)]

• 04049471110043: Single use patient interface for the VisuMax laser keratome
• 04049471100136: single use accessory for ZEISS femtosecond lasers