SURVAC™

GUDID 14063108108644

Suction Catheters for Bronchoscopy PTFE, 2 x 3, L 60

NOVATECH

Suction system catheter, general-purpose

• Primary Device ID: 14063108108644
• NIH Device Record Key: e577a39b-8000-41b7-9b51-fc1c4c9af622
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SURVAC™
• Version Model Number: 77622
• Company DUNS: 777211640
• Company Name: NOVATECH
• 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: false
• 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	14063108108644 [Primary]

FDA Product Code

• BSY: Catheters, Suction, Tracheobronchial

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: 2024-06-26
• Device Publish Date: 2024-06-18

On-Brand Devices [SURVAC™]

• 14063108108675: Suction Catheters for Bronchoscopy PC, 3 x 4, L 30
• 14063108108668: Suction Catheters for Bronchoscopy PC, 3 x 4, L 60
• 14063108108651: Suction Catheters for Bronchoscopy PC, 2 x 2.7, L 60
• 14063108108644: Suction Catheters for Bronchoscopy PTFE, 2 x 3, L 60