Blower Nozzle

GUDID 04560264546172

NAKANISHI INC.

Dental abrasive air jet system handpiece

• Primary Device ID: 04560264546172
• NIH Device Record Key: 7b9acd43-686d-41f2-b2c1-7a69b6aca599
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Blower Nozzle
• Version Model Number: Blower Nozzle-KV (PER)
• Company DUNS: 690710546
• Company Name: NAKANISHI INC.
• 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: false
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: false
• 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	04560264546172 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K241880

FDA Product Code

• EFB: Handpiece, air-powered, dental

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: 2025-03-31
• Device Publish Date: 2025-03-21

On-Brand Devices [Blower Nozzle]

• 04560264546202: Blower Nozzle-M4 (PER)
• 04560264546172: Blower Nozzle-KV (PER)
• 04560264546165: Blower Nozzle-PTL (PER)