SafePath 1F001

GUDID 00861298002608

One pouched device, 1F001

Safepath Medical, Inc.

Silk suture

• Primary Device ID: 00861298002608
• NIH Device Record Key: 319c3fc3-0074-45a2-aee4-0749ad833ed9
• Commercial Distribution Discontinuation: 2023-12-31
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SafePath
• Version Model Number: 1F001
• Catalog Number: 1F001
• Company DUNS: 877189584
• Company Name: Safepath Medical, Inc.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: true
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00861298002608 [Primary]

FDA Product Code

• GAP: Suture, Nonabsorbable, Silk

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: 2022-02-07
• Device Publish Date: 2022-01-28

On-Brand Devices [SafePath]

• 00861298002622: One pouched device, 1F002
• 00861298002608: One pouched device, 1F001