EasyDrill Cranial Perforator Ø9 x Ø6 x 3mm DM0008FAA

GUDID 07898959543166

Micromar Indústria e Comércio Ltda

Automatic cranial perforator, single-use

• Primary Device ID: 07898959543166
• NIH Device Record Key: f8bcf82a-c612-4def-a49e-06a82c52bfea
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: EasyDrill Cranial Perforator Ø9 x Ø6 x 3mm
• Version Model Number: DM0008FAA
• Catalog Number: DM0008FAA
• Company DUNS: 902807742
• Company Name: Micromar Indústria e Comércio Ltda
• 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: 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: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 1-800-433-7080
• Email: xx@xx.xx

Device Dimensions

• Device Size Text, specify: 0

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *Keep dry

Device Identifiers

Device Issuing Agency	Device ID
GS1	07898959543166 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K141455

FDA Product Code

• HBF: Drills, Burrs, Trephines & Accessories (Compound, Powered)

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-04-08
• Device Publish Date: 2020-03-31

On-Brand Devices [EasyDrill Cranial Perforator Ø9 x Ø6 x 3mm]

• 07898959543166: DM0008FAA
• 07898959543500: DM0008FAA
• 07898959543555: DM0008FAA
• 07898959543623: DM0008FAA