DRILL GUIDE SINGLE HOLE

GUDID 00810012484220

BIOPRO, INC.

Surgical depth gauge, single-use

• Primary Device ID: 00810012484220
• NIH Device Record Key: b87343f5-0fa3-40d8-854e-ffdbe81238ca
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DRILL GUIDE SINGLE HOLE
• Version Model Number: 19467
• 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	00810012484220 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K101030

FDA Product Code

• LXH: Orthopedic Manual Surgical Instrument

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: 2019-06-14
• Device Publish Date: 2019-06-06

On-Brand Devices [DRILL GUIDE SINGLE HOLE]

• M20917560: 17656
• 00810012484220: 19467
• 00810012483858: 17656