Beaver-Visitec MMK110/3

GUDID 05055186236069

Malosa Core Suface Treatment Pack (20/SP)

Beaver-Visitec International, Inc.

Ophthalmic surgical procedure kit, non-medicated, single-use

• Primary Device ID: 05055186236069
• NIH Device Record Key: a535b9de-638b-448b-b422-b4895d9ff65d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Beaver-Visitec
• Version Model Number: MMK110/3
• Catalog Number: MMK110/3
• Company DUNS: 001406024
• Company Name: Beaver-Visitec International, Inc.
• Device Count: 20
• 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: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	05055186236069 [Unit of Use]
GS1	35055186236060 [Primary]

FDA Product Code

• PZG: Surgical Eye Tray

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2021-11-23
• Device Publish Date: 2021-11-15

On-Brand Devices [Beaver-Visitec]

• 05055186237981: Malosa Core Phaco Pack 1 (30/SP)
• 05055186236953: Malosa Core SMILE Pack 1 (20/SP)
• 05055186236069: Malosa Core Suface Treatment Pack (20/SP)
• 05055186236052: Malosa Core LASIK Pack 2 (20/SP)
• 05055186235833: Malosa Core Phaco Pack 2 (30/SP)
• 05055186240066: Malosa Core SMILE Pack 2-Beaver-Visitec International Ltd (30/SP)