KV-Adaptor

GUDID 04560264573376

NAKANISHI INC.

Dental handpiece maintenance unit

• Primary Device ID: 04560264573376
• NIH Device Record Key: d1ebac64-fe0c-4b04-b93f-62a0e92a65fb
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: KV-Adaptor
• Version Model Number: KV-Adaptor
• 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: true
• Serial Number: false
• Manufacturing Date: false
• 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	04560264573376 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K081811

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: 2020-07-09
• Device Publish Date: 2020-07-01

Devices Manufactured by NAKANISHI INC.

• 04560264575158 - Nozzle Holder: 2024-11-25
• 04560264575165 - Nozzle Holder: 2024-11-25
• 04560264575172 - Internal Spray Nozzle: 2024-11-25
• 04560264575189 - Cleaning Wire: 2024-11-25
• 04560264575271 - Tube Holder: 2024-11-25
• 04560264576506 - Protection Plug: 2024-11-25
• 04560264576513 - Coolant Solution Hanger Post: 2024-11-25
• 04589551392421 - Tube Holder: 2024-11-25