Sterilizable cap (VISULUX)

GUDID 04049539103529

Carl Zeiss Meditec AG

Medical equipment drape, reusable Medical equipment drape, reusable Medical equipment drape, reusable Medical equipment drape, reusable Medical equipment drape, reusable Medical equipment drape, reusable Medical equipment drape, reusable Medical equipment drape, reusable Medical equipment drape, reusable Medical equipment drape, reusable Medical equipment drape, reusable Medical equipment drape, reusable Medical equipment drape, reusable Medical equipment drape, reusable Medical equipment drape, reusable Medical equipment drape, reusable Medical equipment drape, reusable Medical equipment drape, reusable

• Primary Device ID: 04049539103529
• NIH Device Record Key: 97ac0a21-ade5-4860-9f6c-dd1265c4cff8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Sterilizable cap (VISULUX)
• Version Model Number: 302550-9022-000
• 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: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	04049539103529 [Primary]

FDA Product Code

• PUI: Drape, Surgical, Exempt

Sterilization

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

[04049539103529]

Moist Heat or Steam Sterilization

[04049539103529]

Moist Heat or Steam Sterilization

[04049539103529]

Moist Heat or Steam Sterilization

[04049539103529]

Moist Heat or Steam Sterilization

[04049539103529]

Moist Heat or Steam Sterilization

[04049539103529]

Moist Heat or Steam Sterilization

[04049539103529]

Moist Heat or Steam Sterilization

[04049539103529]

Moist Heat or Steam Sterilization

[04049539103529]

Moist Heat or Steam Sterilization

[04049539103529]

Moist Heat or Steam Sterilization

[04049539103529]

Moist Heat or Steam Sterilization

[04049539103529]

Moist Heat or Steam Sterilization

[04049539103529]

Moist Heat or Steam Sterilization

[04049539103529]

Moist Heat or Steam Sterilization

[04049539103529]

Moist Heat or Steam Sterilization

[04049539103529]

Moist Heat or Steam Sterilization

[04049539103529]

Moist Heat or Steam Sterilization

[04049539103529]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-04-12
• Device Publish Date: 2023-04-04

Devices Manufactured by Carl Zeiss Meditec AG

• 04049471100143 - Treatment Pack (Size M): 2024-02-19 single use accessory for ZEISS femtosecond lasers
• 04049471100150 - Treatment Pack (Size L): 2024-02-19 single use accessory for ZEISS femtosecond lasers
• 04049471100167 - Treatment Pack (Type KP): 2024-02-19 single use accessory for ZEISS femtosecond lasers
• 04049471100136 - Treatment Pack (Size S): 2024-02-16 single use accessory for ZEISS femtosecond lasers
• 04049539101341 - EyeMag Smart: 2023-11-16
• 04049539101358 - EyeMag Pro S: 2023-11-16
• 04049539101365 - EyeMag Pro F: 2023-11-16
• 04049539064103 - PENTERO® 800 S: 2023-09-19