Medacta International Adapter - ACMI 03.52.10.1204

GUDID 00812432020743

LUMITEX, INC.

Surgical instrument fibreoptic light

• Primary Device ID: 00812432020743
• NIH Device Record Key: bf42d395-1f89-430c-854d-e1983545e013
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Medacta International Adapter - ACMI
• Version Model Number: 011204
• Catalog Number: 03.52.10.1204
• 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	00812432020743 [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: 2020-10-08
• Device Publish Date: 2020-09-30

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