VisionGuard® Replacement Lenses

GUDID 04049539102348

Carl Zeiss Meditec AG

Instrument/equipment drape, single-use, sterile

• Primary Device ID: 04049539102348
• NIH Device Record Key: c412f146-2d5e-49be-aa1d-a13bc6c5d6de
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: VisionGuard® Replacement Lenses
• Version Model Number: 306001-0000-000
• Company DUNS: 342228620
• Company Name: Carl Zeiss Meditec AG
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: true
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	04049539101334 [Primary]
GS1	04049539102133 [Package]; Contains: 04049539101334; Package: [20 Units]; In Commercial Distribution
GS1	04049539102348 [Package]; Contains: 04049539102133; Package: [10 Units]; In Commercial Distribution

FDA Product Code

• KKX: Drape, Surgical

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-08-22

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• 04049471100136 - Treatment Pack (Size S): 2024-02-16 single use accessory for ZEISS femtosecond lasers
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• 04049539101358 - EyeMag Pro S: 2023-11-16
• 04049539101365 - EyeMag Pro F: 2023-11-16
• 04049539064103 - PENTERO® 800 S: 2023-09-19