PDO M463

GUDID 10790986006390

C.P. MEDICAL CORPORATION

Polyester suture, bioabsorbable, monofilament, non-antimicrobial

• Primary Device ID: 10790986006390
• NIH Device Record Key: 33bad46e-6356-4884-96a9-32c59d45b9bc
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PDO
• Version Model Number: M463
• Catalog Number: M463
• Company DUNS: 807404611
• Company Name: C.P. MEDICAL CORPORATION
• 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	10790986006390 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K013274

FDA Product Code

• NEW: Suture, Surgical, Absorbable, Polydioxanone

Sterilization

• Steralize Prior To Use: true
• Device Is Sterile: true

[10790986006390]

Ethylene Oxide

[10790986006390]

Ethylene Oxide

[10790986006390]

Ethylene Oxide

[10790986006390]

Ethylene Oxide

[10790986006390]

Ethylene Oxide

[10790986006390]

Ethylene Oxide

[10790986006390]

Ethylene Oxide

[10790986006390]

Ethylene Oxide

[10790986006390]

Ethylene Oxide

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 6
• Public Version Date: 2021-02-05
• Device Publish Date: 2016-02-23

On-Brand Devices [PDO]

• 10790986006390: M463
• 10790986006383: M303