Water Trap

GUDID 04719872104124

A non-sterile device intended to be integrated within a breathing circuit

ENTER MEDICAL CORPORATION

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• Primary Device ID: 04719872104124
• NIH Device Record Key: 45b9080f-e4a1-40c9-a522-1b5701fe82db
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Water Trap
• Version Model Number: ENT-2013
• Company DUNS: 658833116
• Company Name: ENTER MEDICAL CORPORATION
• 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: true
• 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	04719872104124 [Primary]

FDA Product Code

• BYH: Drain, Tee (Water Trap)

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-06-27
• Device Publish Date: 2023-06-19

Devices Manufactured by ENTER MEDICAL CORPORATION

• 04719872100607 - RESERVOIR: 2023-10-27 RESERVOIR
• 04719872101208 - Seal Rite Mask: 2023-10-27 Seal Rite Mask
• 04719872102021 - Catheter Mount: 2023-10-27 Catheter Mount
• 04719872103028 - Bubble Humidifier: 2023-10-27 Bubble Humidifier
• 04719872104414 - Nasal Cannula: 2023-10-27 Nasal Cannula
• 04719872104568 - reusable resuscitator: 2023-10-27 reusable resuscitator
• 04719872109631 - Disposable Resuscitator: 2023-10-27 Disposable Resuscitator
• 04719872109853 - Anaesthetic Face Mask: 2023-10-27 Anaesthetic Face Mask