Mediwish

GUDID 06974409699681

MEDIWISH CO.,LTD

Dental-professional prophylaxis brush, single-use

• Primary Device ID: 06974409699681
• NIH Device Record Key: a037877f-acad-4738-b814-903180c6a6bc
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Mediwish
• Version Model Number: 2.5mm
• Company DUNS: 548204824
• Company Name: MEDIWISH CO.,LTD
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: false
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: true
• 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	06974409699681 [Primary]

FDA Product Code

• KXF: Applicator, Absorbent Tipped, Non-Sterile

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: 2023-03-01
• Device Publish Date: 2023-02-21