VIVIT Supply

GUDID 20810141931071

Medical Face Mask, Ear Loops, Pediatric, Printed, ASTM Level 1

Vivit Supply LLC

Surgical/medical face mask, non-antimicrobial, single-use

• Primary Device ID: 20810141931071
• NIH Device Record Key: 5af3f093-cc3f-4995-aee6-2cd538a2e101
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: VIVIT Supply
• Version Model Number: 10216PM
• Company DUNS: 119042597
• Company Name: Vivit Supply LLC
• Device Count: 50
• DM Exempt: false
• Pre-market Exempt: false
• 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: true
• RX Perscription: false
• OTC Over-The-Counter: false

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *Store in cool, dry, and well ventilated space out of direct sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Store in cool, dry, and well ventilated space out of direct sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Store in cool, dry, and well ventilated space out of direct sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Store in cool, dry, and well ventilated space out of direct sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Store in cool, dry, and well ventilated space out of direct sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Store in cool, dry, and well ventilated space out of direct sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Store in cool, dry, and well ventilated space out of direct sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Store in cool, dry, and well ventilated space out of direct sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Store in cool, dry, and well ventilated space out of direct sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Store in cool, dry, and well ventilated space out of direct sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Store in cool, dry, and well ventilated space out of direct sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Store in cool, dry, and well ventilated space out of direct sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Store in cool, dry, and well ventilated space out of direct sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Store in cool, dry, and well ventilated space out of direct sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Store in cool, dry, and well ventilated space out of direct sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Store in cool, dry, and well ventilated space out of direct sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Store in cool, dry, and well ventilated space out of direct sunlight

Device Identifiers

Device Issuing Agency	Device ID
GS1	00810141931077 [Unit of Use]
GS1	10810141931074 [Primary]
GS1	20810141931071 [Package]; Contains: 10810141931074; Package: Case [10 Units]; In Commercial Distribution

FDA Product Code

• OXY: Balloon Catheter, Redirecting Blood Flow

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: 2023-09-25
• Device Publish Date: 2023-09-15

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