Passio Catheter Valve Replacement Kit

GUDID 10860099001343

Bearpac Medical, LLC

Pleural/peritoneal drainage catheterization kit

• Primary Device ID: 10860099001343
• NIH Device Record Key: ceb2fd8c-9a1d-46fc-a9c5-2a02d14695be
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Passio Catheter Valve Replacement Kit
• Version Model Number: PAS-05
• 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00860099001346 [Primary]
GS1	10860099001343 [Package]; Contains: 00860099001346; Package: Case [10 Units]; In Commercial Distribution

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: 2023-09-04
• Device Publish Date: 2023-08-25

Devices Manufactured by Bearpac Medical, LLC

• 00086000903220 - Passio Redressing Kit: 2024-03-08
• 10860099001398 - Passio Valve Cap Kit: 2024-03-08
• 00860099001308 - Passio Disposable Collection System: 2023-09-04
• 10860099001343 - Passio Catheter Valve Replacement Kit: 2023-09-04
• 10860099001343 - Passio Catheter Valve Replacement Kit: 2023-09-04
• 00860099001322 - Passio Pump Drainage System: 2023-08-21 Starter Pac
• 00860099001353 - Passio Adapter Kit: 2023-08-21