PRO-OPTIONS

GUDID 07350111280031

Pro-Options AB

Hand-held dental retractor

• Primary Device ID: 07350111280031
• NIH Device Record Key: 891343bb-3108-41ff-8333-0283f6da74c3
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PRO-OPTIONS
• Version Model Number: 05053
• Company DUNS: 554775309
• Company Name: Pro-Options AB
• 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: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	07350111280031 [Primary]

FDA Product Code

• EIF: Accessories, Retractor, Dental

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: 2020-07-09
• Device Publish Date: 2020-07-01

On-Brand Devices [PRO-OPTIONS]

• 07350111280048: 05054
• 07350111280031: 05053
• 07350111280246: 8080
• 07350111280253: 8070
• 07350111280260: 8060