Aquilex Fluid Control System AQL-BEMIS

GUDID 10073088152999

Kit containing 36-3000cc canister with aerostat filter, float valve shutoff, 18-18" connecting tubes and 18 specimen collectors

BEMIS MANUFACTURING COMPANY

Surgical suction system collection container, single-use

• Primary Device ID: 10073088152999
• NIH Device Record Key: 7b172d9a-0e3b-4dcd-b92e-0ec881773847
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Aquilex Fluid Control System
• Version Model Number: AQL-BEMIS
• Catalog Number: AQL-BEMIS
• Company DUNS: 006072078
• Company Name: BEMIS MANUFACTURING COMPANY
• Device Count: 36
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: true
• 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: true
• OTC Over-The-Counter: false

Device Dimensions

• Total Volume: 3000 Milliliter
• Total Volume: 3000 Milliliter
• Total Volume: 3000 Milliliter
• Total Volume: 3000 Milliliter
• Total Volume: 3000 Milliliter
• Total Volume: 3000 Milliliter
• Total Volume: 3000 Milliliter
• Total Volume: 3000 Milliliter
• Total Volume: 3000 Milliliter
• Total Volume: 3000 Milliliter
• Total Volume: 3000 Milliliter
• Total Volume: 3000 Milliliter
• Total Volume: 3000 Milliliter
• Total Volume: 3000 Milliliter
• Total Volume: 3000 Milliliter
• Total Volume: 3000 Milliliter
• Total Volume: 3000 Milliliter
• Total Volume: 3000 Milliliter
• Total Volume: 3000 Milliliter
• Total Volume: 3000 Milliliter
• Total Volume: 3000 Milliliter
• Total Volume: 3000 Milliliter
• Total Volume: 3000 Milliliter
• Total Volume: 3000 Milliliter
• Total Volume: 3000 Milliliter
• Total Volume: 3000 Milliliter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00073088152992 [Unit of Use]
GS1	10073088152999 [Primary]

FDA Product Code

• KDQ: Bottle, Collection, Vacuum

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 5
• Public Version Date: 2020-05-06
• Device Publish Date: 2016-09-24

Devices Manufactured by BEMIS MANUFACTURING COMPANY

• 00073088165299 - Bemis: 2025-02-17 3000CC LIPOSUCTION CANISTER W/AEROSTAT FILTER, FLOAT VALVE SHUTOFF, PINK LID
• 00073088165305 - BEMIS: 2025-02-17 2000CC LIPOSUCTION CANISTER W/AEROSTAT FILTER, FLOAT VALVE SHUTOFF, PINK LID
• 00073088162663 - BEMIS: 2024-12-03 2000CC/ML SUCTION CANISTER WITH PPV FILTER, ORANGE LID
• 00073088162649 - BEMIS: 2024-10-31 800CC SUCTION CANISTER WITH PPV FILTER WITH ORANGE LID
• 00073088162656 - BEMIS: 2024-10-23 1200CC SUCTION CANISTER WITH PPV FILTER AND ORANGE LID
• 00073088162670 - BEMIS: 2024-10-23 3000CC SUCTION CANISTER WITH PPV FILTER, ORANGE LID
• 20073088150565 - BEMIS: 2024-10-23 800CC HIFLOW SOLO SUCTION CANISTER WITH AEROSTAT FILTER, FLOAT VALVE SHUTOFF WITH GREEN LID
• 10073088164244 - BEMIS: 2024-05-27 800CC HIFLOW SOLO SUCTION CANISTER WITH AEROSTAT FILTER, FLOAT VALVE SHUTOFF WITH WHITE LID