POWER FIBER

GUDID 20790986004546

C.P. MEDICAL CORPORATION

Polyolefin suture, multifilament

• Primary Device ID: 20790986004546
• NIH Device Record Key: 3ddea0b1-1a4c-4aab-a303-e41c7e24eb06
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: POWER FIBER
• Version Model Number: CPF-P02
• 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	10790986004549 [Primary]
GS1	20790986004546 [Package]; Contains: 10790986004549; Package: [12 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K041894

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: 5
• Public Version Date: 2021-02-05
• Device Publish Date: 2015-09-24

On-Brand Devices [POWER FIBER]

• 20790986004584: CPF-P05A
• 20790986004553: CPF-P026
• 20790986004546: CPF-P02