ForceBraid

GUDID 10818614020065

Suture

RIVERPOINT MEDICAL, LLC

Polyolefin suture, multifilament

• Primary Device ID: 10818614020065
• NIH Device Record Key: 9f62fca4-d758-4f72-b385-90c1c5426e08
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ForceBraid
• Version Model Number: HS311
• Company DUNS: 964053560
• Company Name: RIVERPOINT MEDICAL, LLC
• 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: true
• 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	00818614020068 [Primary]
GS1	10818614020065 [Package]; Contains: 00818614020068; Package: [12 Units]; In Commercial Distribution

FDA Product Code

• GAT: Suture, Nonabsorbable, Synthetic, Polyethylene

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-03-12
• Device Publish Date: 2020-03-04

On-Brand Devices [ForceBraid]

• 10812444029212: Suture Tape
• 10812444029205: Suture Tape
• 10818614020089: Suture
• 10818614020072: Suture
• 10818614020065: Suture
• 10818614020058: Suture
• 10818614020041: Suture
• 10818614020034: Suture
• 10818614020027: Suture
• 10818614020010: Suture
• 10818614020003: Suture
• 10810020083023: Suture
• 10840277401813: Suture