Coag it NASAL PACK

GUDID 00860003566534

Coag it NASAL PACK (dual pouch, single unit)

COAGCO LLC

Intranasal splint, non-biodegradable

• Primary Device ID: 00860003566534
• NIH Device Record Key: dd695974-cc62-4d66-bbd4-242a9eb97a9a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Coag it NASAL PACK
• Version Model Number: CC0009A
• Company DUNS: 083472251
• Company Name: COAGCO LLC
• 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: 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	00860003566534 [Primary]
GS1	10860003566531 [Package]; Package: Case [10 Units]; In Commercial Distribution

FDA Product Code

• EMX: Balloon, Epistaxis

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-04-13
• Device Publish Date: 2023-04-05