Ventix® 110025999

GUDID M543110025999

CAYENNE MEDICAL, INC.

Bone awl

• Primary Device ID: M543110025999
• NIH Device Record Key: 02dc0de7-359b-4428-950d-0f1956d7edfe
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Ventix®
• Version Model Number: 110025999
• Catalog Number: 110025999
• 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: false
• 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
HIBCC	M543110025999 [Primary]

FDA Product Code

• HWJ: Awl

Sterilization

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

[M543110025999]

Moist Heat or Steam Sterilization

[M543110025999]

Moist Heat or Steam Sterilization

[M543110025999]

Moist Heat or Steam Sterilization

[M543110025999]

Moist Heat or Steam Sterilization

[M543110025999]

Moist Heat or Steam Sterilization

[M543110025999]

Moist Heat or Steam Sterilization

[M543110025999]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2019-04-29
• Device Publish Date: 2019-04-19

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