HS Suture Tape

GUDID 00810020082074

Suture

RIVERPOINT MEDICAL, LLC

Polyolefin suture, multifilament

• Primary Device ID: 00810020082074
• NIH Device Record Key: 9c319720-8375-40c8-9467-78d88a590ced
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: HS Suture Tape
• Version Model Number: AO-HS320
• 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	00810020082074 [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: 2019-11-14
• Device Publish Date: 2019-11-06

On-Brand Devices [HS Suture Tape]

• 00812444027471: Suture
• 10812444026754: Suture
• 10812444026747: Suture
• 10812444026730: Suture
• 10812444026723: Suture
• 10812444026716: Suture
• 10812444026709: Suture
• 20812444024412: SUTURE
• 00810020082074: Suture
• 00810020081923: Suture
• 00810020080834: Suture