SurgiPoint

GUDID 10840277402933

Suture.

RIVERPOINT MEDICAL, LLC

Polyester suture, bioabsorbable, monofilament, non-antimicrobial Polyester suture, bioabsorbable, monofilament, non-antimicrobial Polyester suture, bioabsorbable, monofilament, non-antimicrobial Polyester suture, bioabsorbable, monofilament, non-antimicrobial Polyester suture, bioabsorbable, monofilament, non-antimicrobial Polyester suture, bioabsorbable, monofilament, non-antimicrobial Polyester suture, bioabsorbable, monofilament, non-antimicrobial Polyester suture, bioabsorbable, monofilament, non-antimicrobial Polyester suture, bioabsorbable, monofilament, non-antimicrobial Polyester suture, bioabsorbable, monofilament, non-antimicrobial Polyester suture, bioabsorbable, monofilament, non-antimicrobial Polyester suture, bioabsorbable, monofilament, non-antimicrobial Polyester suture, bioabsorbable, monofilament, non-antimicrobial Polyester suture, bioabsorbable, monofilament, non-antimicrobial Polyester suture, bioabsorbable, monofilament, non-antimicrobial Polyester suture, bioabsorbable, monofilament, non-antimicrobial Polyester suture, bioabsorbable, monofilament, non-antimicrobial

• Primary Device ID: 10840277402933
• NIH Device Record Key: dba312a1-d00e-4adc-9dbd-52ed90fe449d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SurgiPoint
• Version Model Number: Q401
• Company DUNS: 964053560
• Company Name: RIVERPOINT MEDICAL, LLC
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Safe
• 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	00840277402936 [Primary]
GS1	10840277402933 [Package]; Contains: 00840277402936; Package: [12 Units]; In Commercial Distribution

FDA Product Code

• GAM: Suture, Absorbable, Synthetic, Polyglycolic Acid

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: 2023-12-13
• Device Publish Date: 2023-12-05

On-Brand Devices [SurgiPoint]

• 10812444028987: Suture
• 10812444028970: Suture
• 10812444028901: Suture
• 10812444028895: Suture
• 10812444028888: Suture
• 10812444028352: Suture
• 10812444028109: Suture
• 10812444028093: Suture
• 10812444027959: Suture
• 10812444027423: Suture
• 10812444027416: SUTURE
• 10812444027393: Suture
• 10812444027072: Suture
• 10812444026440: SUTURE
• 10812444026433: SUTURE
• 10812444026099: SUTURE
• 10812444026082: SUTURE
• 10812444025993: SUTURE
• 10812444024491: SUTURE
• 10812444020493: SUTURE
• 10812444020486: SUTURE
• 10812444020424: SUTURE
• 10812444020417: SUTURE
• 10812444020400: SUTURE
• 10812444020394: SUTURE
• 10812444020387: SUTURE
• 10812444020370: SUTURE
• 10812444020363: SUTURE
• 10812444020356: SUTURE
• 10812444020349: SUTURE
• 10812444020332: SUTURE
• 10812444020325: SUTURE
• 10812444020318: SUTURE
• 10812444020301: SUTURE
• 10812444020295: SUTURE
• 10812444020288: SUTURE
• 10812444020271: SUTURE
• 10812444020264: SUTURE
• 10812444020257: SUTURE
• 10812444020240: SUTURE
• 10812444020233: SUTURE
• 10812444020226: SUTURE
• 10812444020219: SUTURE
• 10812444020202: SUTURE
• 00812444020175: SUTURE
• 00812444020151: SUTURE
• 00812444020144: SUTURE
• 00812444020137: Suture
• 00812444020120: Suture
• 10812444020110: SUTURE