CYTOSURG

GUDID 10812444020066

SUTURE

RIVERPOINT MEDICAL, LLC

Polytetrafluoroethylene suture Polytetrafluoroethylene suture

• Primary Device ID: 10812444020066
• NIH Device Record Key: 80dc9006-db25-429d-abdd-0583773ce3f4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CYTOSURG
• Version Model Number: T8682
• 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: 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	00812444020069 [Primary]
GS1	10812444020066 [Package]; Contains: 00812444020069; Package: [12 Units]; In Commercial Distribution

FDA Product Code

• NBY: Suture, Surgical, Nonabsorbable, Expanded, Polytetraflouroethylene

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2015-10-22

On-Brand Devices [CYTOSURG]

• 10812444020097: SUTURE
• 10812444020080: SUTURE
• 10812444020073: SUTURE
• 10812444020066: SUTURE
• 10812444020059: SUTURE
• 10812444020042: SUTURE
• 10812444020035: SUTURE
• 10812444020028: SUTURE
• 10812444020011: SUTURE
• 10810020084662: Suture
• 10810020084655: Suture
• 10810020084648: Suture
• 10810020084631: Suture
• 10810020084624: Suture
• 10810020084617: Suture
• 10810020084600: Suture
• 00810020084597: Suture
• 10810020084587: Suture