PRO-OPTIONS

GUDID 07350111280246

Pro-Options AB

Rubber dam, non-latex

• Primary Device ID: 07350111280246
• NIH Device Record Key: 1b679336-33fd-4667-9d02-a32e5d5a728b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PRO-OPTIONS
• Version Model Number: 8080
• Company DUNS: 554775309
• Company Name: Pro-Options AB
• Device Count: 20
• 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: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	07350111280024 [Primary]
GS1	07350111280246 [Unit of Use]

FDA Product Code

• EIE: Dam, Rubber

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