532nm LIO

GUDID 05055272719674

KEELER LIMITED

Indirect binocular laser ophthalmoscope

• Primary Device ID: 05055272719674
• NIH Device Record Key: 9d8c23d6-170e-46b1-9d0d-3629cab2de28
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: 532nm LIO
• Version Model Number: 1205-P-2130
• Company DUNS: 210164398
• Company Name: KEELER LIMITED
• 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	05055272719674 [Primary]

FDA Product Code

• HQF: Laser, Ophthalmic

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: 2021-07-28
• Device Publish Date: 2021-07-20

Devices Manufactured by KEELER LIMITED

• 05055272707503 - ADAPTOR FOR F SIZE CO2 CYLINDER: 2025-04-03
• 05055272707527 - ADAPTOR FOR F SIZE N2O CYLINDER: 2025-04-03
• 05055272721424 - DORC CRYOSTAR ADAPTOR: 2025-04-03
• 05055272721431 - ERBE ERBOKRYO ADAPTOR: 2025-04-03
• 05055272719674 - 532nm LIO: 2021-07-28
• 05055272719674 - 532nm LIO: 2021-07-28
• 05055272720328 - 514/810nm LIO: 2021-07-28
• 05055272720380 - 577nm LIO: 2021-07-28
• 05055272719926 - 3.6V PROFESSIONAL OPHTH IN CASE: 2020-03-06