CARDIOXYL®

GUDID 03661522103142

PETERS SURGICAL

Polyester suture, non-bioabsorbable, multifilament

• Primary Device ID: 03661522103142
• NIH Device Record Key: 14d661a0-1f23-4ce1-abc3-494e3e226430
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CARDIOXYL®
• Version Model Number: 73PK30EG
• Company DUNS: 265741780
• Company Name: PETERS SURGICAL
• 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	03661522103142 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K060163

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: 2026-03-13
• Device Publish Date: 2026-03-05

On-Brand Devices [CARDIOXYL®]

• 03661522103142: 73PK30EG
• 03661522101391: 73S20Y
• 03661522101285: 73I30R
• 03661522100851: 73P30EF
• 03661522100844: 73S30EA
• 03661522100837: 73P30DK