LERNA

GUDID 00896180011741

Skin Protectant Prep Pad

Lernapharm (Loris) Inc

Skin adhesive protective material

• Primary Device ID: 00896180011741
• NIH Device Record Key: 751f6e91-6b21-462d-812b-89bc35980b87
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LERNA
• Version Model Number: 222-01
• Company DUNS: 206940905
• Company Name: Lernapharm (Loris) 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• 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	00896180011741 [Primary]

FDA Product Code

• NEC: Bandage, Liquid, Skin Protectant

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2021-02-05
• Device Publish Date: 2021-01-28