BioWick SureLock® CM-6120

GUDID M543CM6120

CAYENNE MEDICAL, INC.

Surgical drill guide, reusable

• Primary Device ID: M543CM6120
• NIH Device Record Key: dbc9bca8-44c2-4aae-9bed-80266a68e816
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: BioWick SureLock®
• Version Model Number: CM-6120
• Catalog Number: CM-6120
• 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	M543CM6120 [Primary]

FDA Product Code

• NBH: Accessories, Arthroscopic

Sterilization

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

[M543CM6120]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2020-04-06
• Device Publish Date: 2019-03-29

On-Brand Devices [BioWick SureLock®]

• M543CM6121: CM-6121
• M543CM6120: CM-6120
• M543CM6101: CM-6101
• M543CM6101H1: CM-6101H
• 00887868269752: CM-6121
• 00887868269745: CM-6120
• 00887868269738: CM-6101H
• 00887868269721: CM-6101