Hurri-Freeze

GUDID 20723797809444

Hurri-Freeze Topical Anesthetic Spray - 35mL Mist

BEUTLICH PHARMACEUTICALS, LLC

General cryosurgical system, cryogen gas, mechanical

• Primary Device ID: 20723797809444
• NIH Device Record Key: 84334aa1-66fe-49ce-97f5-b4c1851a2b1d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Hurri-Freeze
• Version Model Number: 35mL Mist
• Company DUNS: 005209325
• Company Name: BEUTLICH PHARMACEUTICALS, LLC
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• 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	10723797809447 [Primary]
GS1	20723797809444 [Package]; Contains: 10723797809447; Package: case [24 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K232674

FDA Product Code

• MLY: Vapocoolant Device

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: 2025-12-23
• Device Publish Date: 2025-12-15

On-Brand Devices [Hurri-Freeze]

• 20723797809444: Hurri-Freeze Topical Anesthetic Spray - 35mL Mist
• 10723797808440: Hurri-Freeze Topical Anesthetic Spray - 35mL Medium Stream
• 20723797807440: Hurri-Freeze Topical Anesthetic Spray - 115mL Medium Stream
• 20723797806443: Hurri-Freeze Topical Anesthetic Spray - 115mL Mist