CuffTape

GUDID 00810020082913

suture

RIVERPOINT MEDICAL, LLC

Polyolefin suture, multifilament

• Primary Device ID: 00810020082913
• NIH Device Record Key: cf288547-e18a-44d0-b1f5-dd75831f299c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CuffTape
• Version Model Number: HS207
• 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	00810020082913 [Primary]

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: 2020-02-05
• Device Publish Date: 2020-01-28

On-Brand Devices [CuffTape]

• 10812444028932: Suture
• 10812444027188: Suture
• 10812444027171: Suture
• 00810020082913: suture
• 10810020085058: Suture
• 10810020085041: Suture
• 10810020081883: Suture