Curaplex 8600-01299

GUDID 00817617029719

*Custom* TRI ANIM Curaplex Vent Connector Kit

BOUND TREE MEDICAL, LLC

Breathing circuit condensate trap, reusable

• Primary Device ID: 00817617029719
• NIH Device Record Key: 7cd74969-fccc-45d1-beb7-7d4ca6491506
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Curaplex
• Version Model Number: 8600-01299
• Catalog Number: 8600-01299
• Company DUNS: 070556204
• Company Name: BOUND TREE MEDICAL, LLC
• Device Count: 1
• DM Exempt: true
• 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00817617029719 [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: 2019-01-15
• Device Publish Date: 2018-12-15

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