AngioSystems Towel

GUDID 00816611021118

ANGIOSYSTEMS, INCORPORATED

Surgical drape clip Surgical drape clip Surgical drape clip Surgical drape clip, reusable Surgical drape clip, reusable Surgical drape clip, reusable Surgical drape clip, reusable Surgical drape clip, reusable Surgical drape clip, reusable Surgical drape clip, reusable Surgical drape clip, reusable Surgical drape clip, reusable Surgical drape clip, reusable Surgical drape clip, reusable Surgical drape clip, reusable Surgical drape clip, reusable Surgical drape clip, reusable

• Primary Device ID: 00816611021118
• NIH Device Record Key: e2de8cef-85a7-4d7c-9d1c-a1afb7fe68ac
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: AngioSystems Towel
• Version Model Number: 1002-2
• Company DUNS: 144884467
• Company Name: ANGIOSYSTEMS, INCORPORATED
• Device Count: 1
• 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	00816611020395 [Primary]
GS1	00816611021118 [Package]; Contains: 00816611020395; Package: [100 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K843260

FDA Product Code

• KKX: Drape, Surgical

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: 2016-06-15

On-Brand Devices [AngioSystems Towel]

• 00816611021064: SB017026
• 00816611021125: 1032-01
• 00816611021118: 1002-2