AutoDrop

GUDID 00384706050010

Autodrop device in a bag

OWEN MUMFORD USA INCORPORATED

Eye dropper bottle aid

• Primary Device ID: 00384706050010
• NIH Device Record Key: d974df6f-82ca-400a-bbd7-dee9cb4f78a9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: AutoDrop
• Version Model Number: OP 6050
• 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	00384706050010 [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 [AutoDrop]

• 00384706000022: AutoDrop Eye Guide
• 00384706050010: Autodrop device in a bag