CYTOSURG

GUDID 00810020084597

Suture

RIVERPOINT MEDICAL, LLC

Polyolefin suture, monofilament

• Primary Device ID: 00810020084597
• NIH Device Record Key: 8dcbb30d-ef6d-45fa-865f-229ffd0e4551
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CYTOSURG
• Version Model Number: T8001C
• 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	00810020084597 [Primary]
GS1	10810020084594 [Package]; 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: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-09-09
• Device Publish Date: 2020-09-01

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