Ventix® 110026003

GUDID 00887868269431

CAYENNE MEDICAL, INC.

Fluted surgical drill bit, single-use

• Primary Device ID: 00887868269431
• NIH Device Record Key: 0fc79b4d-4350-4f8d-87f8-57b7d62bfefa
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Ventix®
• Version Model Number: 110026003
• Catalog Number: 110026003
• Company DUNS: 606719685
• Company Name: CAYENNE MEDICAL, INC.
• 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00887868269431 [Primary]
HIBCC	M543110026003 [Previous]

FDA Product Code

• HTW: Bit, Drill

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: 2020-09-29
• Device Publish Date: 2020-09-21

On-Brand Devices [Ventix®]

• M543110026003: 110026003
• M543110026002: 110026002
• M543110026001: 110026001
• M543110026000: 110026000
• M543110025998: 110025998
• M543110025999: 110025999
• 00887868348365: 110025999
• 00887868269431: 110026003
• 00887868269424: 110026002
• 00887868269417: 110026001
• 00887868269400: 110026000
• 00887868269394: 110025998