QD-J B2/B3

GUDID 04560264573918

NAKANISHI INC.

Pneumatic dental handpiece coupler

• Primary Device ID: 04560264573918
• NIH Device Record Key: e7a3c34c-d955-4d76-8a7f-d40f716d037f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: QD-J B2/B3
• Version Model Number: QD-J B2/B3
• 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: true
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	04560264573918 [Primary]

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: 2021-12-29
• Device Publish Date: 2021-12-21

On-Brand Devices [QD-J B2/B3]

• 04560264573918: QD-J B2/B3
• 04560264568792: QD-J B2/B3