MicroSlad™ 719 Lens Slide 200 mm AA0192900

GUDID 07290109147000

LUMENIS LTD.

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• Primary Device ID: 07290109147000
• NIH Device Record Key: 8ed73bb2-dd28-468f-9b49-a564903bd36f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MicroSlad™ 719 Lens Slide 200 mm
• Version Model Number: 19101
• Catalog Number: AA0192900
• Company DUNS: 600166524
• Company Name: LUMENIS LTD.
• 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: 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	07290109147000 [Primary]

FDA Product Code

• GEX: Powered Laser Surgical Instrument

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2022-09-12
• Device Publish Date: 2022-09-04

On-Brand Devices [MicroSlad™ 719 Lens Slide 200 mm ]

• 07290109141688: 19101
• 07290109147000: 19101