Vilex AVID Drill AZDL20

GUDID 00841731121103

Drill, AVID 2.0mm QC

VILEX IN TENNESSEE, INC.

Fluted surgical drill bit, single-use, non-sterile

• Primary Device ID: 00841731121103
• NIH Device Record Key: bdcf65b5-d6c3-40f5-b3f1-017fe2f8bc70
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Vilex AVID Drill
• Version Model Number: AZDL20
• Catalog Number: AZDL20
• Company DUNS: 152008371
• Company Name: VILEX IN TENNESSEE, 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: true
• Lot Batch: true
• Serial Number: false
• 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	00841731121103 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K041287

FDA Product Code

• HTW: Bit, Drill

Sterilization

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

[00841731121103]

Moist Heat or Steam Sterilization

[00841731121103]

Moist Heat or Steam Sterilization

[00841731121103]

Moist Heat or Steam Sterilization

[00841731121103]

Moist Heat or Steam Sterilization

[00841731121103]

Moist Heat or Steam Sterilization

[00841731121103]

Moist Heat or Steam Sterilization

[00841731121103]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-11-22
• Device Publish Date: 2018-08-06

On-Brand Devices [Vilex AVID Drill]

• 00841731121165: Drill, AVID 2.5mm QC
• 00841731121103: Drill, AVID 2.0mm QC