Lumitex Surgical Light Cable 005366

GUDID 00812432020200

LUMITEX, INC.

Surgical instrument fibreoptic light

• Primary Device ID: 00812432020200
• NIH Device Record Key: 1eb6a6cc-ebdf-428d-8afc-4a91daf95a1e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Lumitex Surgical Light Cable
• Version Model Number: 005366
• Catalog Number: 005366
• Company DUNS: 108631797
• Company Name: LUMITEX, INC.
• Device Count: 1
• 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: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00812432020200 [Primary]

FDA Product Code

• FDG: Retractor, Fiberoptic

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: 2019-11-05
• Device Publish Date: 2019-10-28

On-Brand Devices [Lumitex Surgical Light Cable]

• 00812432020255: 006424
• 00812432020248: 006423
• 00812432020231: 006422
• 00812432020224: 006241
• 00812432020217: 005757
• 00812432020200: 005366
• 00812432020194: 005365