OCULAR SHIELD

GUDID 13700773724755

OCULAR SHIELD

FCI S A S FCI 20 22

Surgical eye pressure shield

• Primary Device ID: 13700773724755
• NIH Device Record Key: 11332873-2353-4b63-879d-706c2004367d
• Commercial Distribution Discontinuation: 2025-03-23
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: OCULAR SHIELD
• Version Model Number: S6.2301
• Company DUNS: 763408366
• Company Name: FCI S A S FCI 20 22
• 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: true
• Lot Batch: true
• Serial Number: true
• Manufacturing Date: true
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	13700773724755 [Primary]

FDA Product Code

• HOY: Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear)

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2025-03-25
• Device Publish Date: 2021-05-30

On-Brand Devices [OCULAR SHIELD ]

• 13700773724755: OCULAR SHIELD
• 13700773727503: OCULAR SHIELD