Curaplex 670277-KIT

GUDID 00810094576363

Curaplex Air-Q sp3G ALS Kit Size 3 with NG Tube, ET Tube Holder, and Lube Jelly

BOUND TREE MEDICAL, LLC

Oropharyngeal airway, single-use

• Primary Device ID: 00810094576363
• NIH Device Record Key: 7bdf2b2f-4faa-4601-9654-a5699d8cf873
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Curaplex
• Version Model Number: 670277-KIT
• Catalog Number: 670277-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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00810094576363 [Primary]

FDA Product Code

• CAE: AIRWAY, OROPHARYNGEAL, ANESTHESIOLOGY

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: 2023-11-20
• Device Publish Date: 2023-11-10

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