Spineart Storz Cable Adaptor 008657

GUDID 00812432022945

Lumitex, Inc.

Fibreoptic light cable

• Primary Device ID: 00812432022945
• NIH Device Record Key: 3a0521fe-814f-42e4-8fe8-5489c2d8333f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Spineart Storz Cable Adaptor
• Version Model Number: MIS-IN 44 50-N
• Catalog Number: 008657
• 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	00812432022945 [Primary]

FDA Product Code

• FDG: Retractor, Fiberoptic

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2026-01-30
• Device Publish Date: 2023-08-11

On-Brand Devices [Spineart Storz Cable Adaptor]

• 00812432021559: MIS-IN 44 50-N
• 00812432022945: MIS-IN 44 50-N