AutoSqueeze

GUDID 00384706150017

Autosqueeze eyedrop aid device in a bag

OWEN MUMFORD USA INCORPORATED

Eye dropper bottle aid

• Primary Device ID: 00384706150017
• NIH Device Record Key: 6f50c081-9845-4e13-9baa-0b2c39c30f17
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: AutoSqueeze
• Version Model Number: OP 6150
• Company DUNS: 803401454
• Company Name: OWEN MUMFORD USA INCORPORATED
• 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: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	00384706150017 [Primary]

FDA Product Code

• KCM: Dropper, Ent

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: 2023-06-28
• Device Publish Date: 2023-06-20

On-Brand Devices [AutoSqueeze]

• 00384706100012: AutoSqueeze Eye Guide
• 00384706150017: Autosqueeze eyedrop aid device in a bag