FASTRACT

GUDID 00366975058560

BENCO DENTAL SUPPLY CO.

General oral wound dressing, non-animal-derived, sterile

• Primary Device ID: 00366975058560
• NIH Device Record Key: b43e17b7-d627-4952-b784-1daf15144408
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: FASTRACT
• Version Model Number: 4821-383
• Company DUNS: 015108087
• Company Name: BENCO DENTAL SUPPLY CO.
• 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: true
• Lot Batch: true
• Serial Number: true
• 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	00366975058560 [Primary]

FDA Product Code

• MGQ: Dressing, Wound And Burn, Hydrogel W/Drug And/Or Biologic

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: 2022-08-12
• Device Publish Date: 2022-08-04

On-Brand Devices [FASTRACT]

• 00366975013422: FAS-TRACT Epinephrine #2 Knitted Retraction Cord 100 inches
• 00366975013415: FAS-TRACT™ Epinephrine #1 Knitted Retraction Cord 100 inches
• 00366975058560: 4821-383
• 00366975034731: 5455-509