TopLock

GUDID 10810020082286

Suture

RIVERPOINT MEDICAL, LLC

Polyolefin suture, multifilament

• Primary Device ID: 10810020082286
• NIH Device Record Key: 1d0da22d-ec0a-494f-8dcc-253913d23faf
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: TopLock
• Version Model Number: HS100
• 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	00810020082289 [Primary]
GS1	10810020082286 [Package]; Contains: 00810020082289; 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: 2020-03-19
• Device Publish Date: 2020-03-11

On-Brand Devices [TopLock]

• 10810020082316: Suture
• 10810020082309: Suture
• 10810020082293: Suture
• 10810020082286: Suture