MaxBraid PE Suture

GUDID 10840277404265

Suture

RIVERPOINT MEDICAL, LLC

Polyolefin/fluoropolymer suture, multifilament

• Primary Device ID: 10840277404265
• NIH Device Record Key: 85787b0d-9a6c-4e16-9985-fac31efdf53a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MaxBraid PE Suture
• Version Model Number: ZB-HS112
• 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	00840277404268 [Primary]
GS1	10840277404265 [Package]; Contains: 00840277404268; Package: [12 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: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-11-01
• Device Publish Date: 2024-10-24

On-Brand Devices [MaxBraid PE Suture]

• 00840277404299: Suture
• 10840277404289: Suture
• 10840277404272: Suture
• 10840277404265: Suture
• 10840277404258: Suture
• 10840277404241: Suture
• 10840277404234: Suture
• 10840277404227: Suture
• 10840277404210: Suture
• 10840277404203: Suture