Cyclophotocoagulation Probe

GUDID 00853386006735

LIGHTMED USA INC

Ophthalmic fibreoptic light instrument, single-use

• Primary Device ID: 00853386006735
• NIH Device Record Key: 17ad3a98-4400-4826-bd4e-c49e024e85cc
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Cyclophotocoagulation Probe
• Version Model Number: 620231
• Company DUNS: 162060383
• Company Name: LIGHTMED USA INC
• 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: 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00853386006735 [Primary]

FDA Product Code

• MPA: Endoilluminator

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: 2023-07-06
• Device Publish Date: 2023-06-28

Devices Manufactured by LIGHTMED USA INC

• 00853386006735 - Cyclophotocoagulation Probe: 2023-07-06
• 00853386006735 - Cyclophotocoagulation Probe: 2023-07-06
• 00853386006285 - LIGHTSonic B UBM: 2018-07-06