Curaplex 680123-KIT

GUDID 00815277029353

Curaplex Kit - NPA 28 Fr, Latex Free, PVC w/Lube

BOUND TREE MEDICAL, LLC

Nasopharyngeal airway, single-use

• Primary Device ID: 00815277029353
• NIH Device Record Key: 531972eb-1e99-47ad-82df-e6bbb897c861
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Curaplex
• Version Model Number: 680123-KIT
• Catalog Number: 680123-KIT
• 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	00810094571856 [Package]; Package: CS [100 Units]; In Commercial Distribution
GS1	00815277029353 [Primary]

FDA Product Code

• BTQ: AIRWAY, NASOPHARYNGEAL

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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