HS SUTURE TAPE

GUDID 10812444026723

Suture

RIVERPOINT MEDICAL, LLC

Polyolefin suture, multifilament

• Primary Device ID: 10812444026723
• NIH Device Record Key: 8e770ce8-78c5-4019-b0b1-98d89580b640
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: HS SUTURE TAPE
• Version Model Number: HS209
• 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00812444026726 [Primary]
GS1	10812444026723 [Package]; Contains: 00812444026726; Package: [6 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: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2019-02-07
• Device Publish Date: 2017-07-19

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