DRILL GUIDE 3 LEG 10X8

GUDID 00810012484015

BIOPRO, INC.

Surgical drill guide, single-use

• Primary Device ID: 00810012484015
• NIH Device Record Key: 9cec3f04-0914-4f7d-a782-3c35f0d77e7b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DRILL GUIDE 3 LEG 10X8
• Version Model Number: 18302
• Company DUNS: 618749857
• Company Name: BIOPRO, 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: true
• 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	00810012484015 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K072298

FDA Product Code

• FZX: Guide, Surgical, Instrument

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2019-08-09
• Device Publish Date: 2019-06-06

On-Brand Devices [DRILL GUIDE 3 LEG 10X8]

• M209183020: 18302
• 00810012484015: 18302