LUMENIS 100270A50.J V31

GUDID 08056098471613

COSTRUZIONI STRUMENTI OFTALMICI C.S.O. SRL

Ophthalmic slit lamp, examination Ophthalmic slit lamp, examination Ophthalmic slit lamp, examination Ophthalmic slit lamp, examination Ophthalmic slit lamp, examination Ophthalmic slit lamp, examination Ophthalmic slit lamp, examination Ophthalmic slit lamp, examination Ophthalmic slit lamp, examination Ophthalmic slit lamp, examination Ophthalmic slit lamp, examination Ophthalmic slit lamp, examination Ophthalmic slit lamp, examination Ophthalmic slit lamp, examination Ophthalmic slit lamp, examination Ophthalmic slit lamp, examination Ophthalmic slit lamp, examination Ophthalmic slit lamp, examination Ophthalmic slit lamp, examination Ophthalmic slit lamp, examination Ophthalmic slit lamp, examination Ophthalmic slit lamp, examination Ophthalmic slit lamp, examination Ophthalmic slit lamp, examination Ophthalmic slit lamp, examination Ophthalmic slit lamp, examination Ophthalmic slit lamp, examination Ophthalmic slit lamp, examination Ophthalmic slit lamp, examination Ophthalmic slit lamp, examination Ophthalmic examination slit lamp Ophthalmic examination slit lamp Ophthalmic examination slit lamp Ophthalmic examination slit lamp Ophthalmic examination slit lamp Ophthalmic examination slit lamp Ophthalmic examination slit lamp Ophthalmic examination slit lamp Ophthalmic examination slit lamp Ophthalmic examination slit lamp Ophthalmic examination slit lamp Ophthalmic examination slit lamp Ophthalmic examination slit lamp Ophthalmic examination slit lamp Ophthalmic examination slit lamp Ophthalmic examination slit lamp Ophthalmic examination slit lamp

• Primary Device ID: 08056098471613
• NIH Device Record Key: 9300b349-76c8-4490-be12-649583b631ed
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LUMENIS
• Version Model Number: SL 9900 5X
• Catalog Number: 100270A50.J V31
• Company DUNS: 432448470
• Company Name: COSTRUZIONI STRUMENTI OFTALMICI C.S.O. SRL
• 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	08056098471613 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K992836

FDA Product Code

• HJO: Biomicroscope, Slit-Lamp, Ac-Powered

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: 2020-12-18
• Device Publish Date: 2020-12-10

On-Brand Devices [LUMENIS]

• 08056098471613: SL 9900 5X
• 08056098471415: SL 9900 5X digital
• 08056098470869: SL 9800 5X
• 08056098470043: SL 990 5X/Z LUMENIS
• 08056098470036: SL 990 5X LUMENIS
• 8056098470609: SL 990 3X LUMENIS