iPRO

GUDID 05060654200114

iPRO ELITE - SKINTACT Eye Protector

FANNIN (UK) LIMITED

Eye patch

• Primary Device ID: 05060654200114
• NIH Device Record Key: 7ba3d8a1-daf1-4aa8-b771-99e6649de69a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: iPRO
• Version Model Number: FHCEP3
• Company DUNS: 770174886
• Company Name: FANNIN (UK) LIMITED
• Device Count: 100
• 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: 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	05060654200114 [Primary]
GS1	05060654200671 [Unit of Use]

FDA Product Code

• KGX: Tape And Bandage, Adhesive

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: 2023-03-03
• Device Publish Date: 2023-02-23