PTL-CL-FV-T

GUDID 04560264573130

NAKANISHI INC.

Pneumatic dental handpiece coupler

• Primary Device ID: 04560264573130
• NIH Device Record Key: 93553b89-94dd-479d-afbf-c8ff8e3274b0
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PTL-CL-FV-T
• Version Model Number: PTL-CL-FV-T
• 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	04560264573130 [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: 2020-07-24
• Device Publish Date: 2020-07-16

On-Brand Devices [PTL-CL-FV-T]

• 04560264573130: PTL-CL-FV-T
• 04560264568785: PTL-CL-FV-T