Passio Redressing Kit

GUDID 00860009032200

Bearpac Medical, LLC

Pleural/peritoneal drainage catheterization kit

• Primary Device ID: 00860009032200
• NIH Device Record Key: 05afff87-34f1-42ff-90cb-e4213fb686e4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Passio Redressing Kit
• Version Model Number: PAS-02
• Company DUNS: 081178202
• Company Name: Bearpac Medical, LLC
• 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: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00860009032200 [Primary]

FDA Product Code

• DWM: Apparatus, Suction, Patient Care

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: 2025-08-18
• Device Publish Date: 2025-08-08

On-Brand Devices [Passio Redressing Kit]

• 00086000903220: PAS-02
• 00860009032200: PAS-02