Peanut

GUDID 20749915000708

Peanut 3/8" Strung

AMERICAN SURGICAL COMPANY, LLC

Dissection sponge

• Primary Device ID: 20749915000708
• NIH Device Record Key: 07397e2f-a475-4e04-ac82-e7dbcebad1ff
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Peanut
• Version Model Number: 40-03A
• Company DUNS: 151054954
• Company Name: AMERICAN SURGICAL COMPANY, LLC
• Device Count: 40
• DM Exempt: false
• Pre-market Exempt: false
• 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	10749915000701 [Unit of Use]
GS1	20749915000708 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K872809

FDA Product Code

• GDY: Gauze/Sponge, Internal, X-Ray Detectable

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-06-30

On-Brand Devices [Peanut]

• 20749915000708: Peanut 3/8" Strung
• 20749915000692: Peanut 3/8" in Holder