MICROCUT MANUAL 0005000007

GUDID 07897990302343

Microcut Manual - 1 unit (EN/FR)

TDV DENTAL LTDA

Interproximal reduction kit

• Primary Device ID: 07897990302343
• NIH Device Record Key: 0067a8df-dbb0-4bfa-9d3a-5c370ceb25d2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MICROCUT MANUAL
• Version Model Number: 0005000007
• Catalog Number: 0005000007
• Company DUNS: 900580358
• Company Name: TDV DENTAL LTDA
• 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: true
• Serial Number: false
• Manufacturing Date: false
• 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	07897990302343 [Primary]

FDA Product Code

• EKD: Instrument, Cutting, Operative

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: 2025-03-12
• Device Publish Date: 2025-03-04

On-Brand Devices [MICROCUT MANUAL]

• 07897990311789: Microcut Manual - 10 units (EN/FR)
• 07897990302343: Microcut Manual - 1 unit (EN/FR)