GEO

GUDID B504OM222100230

Provision

Drilling power tool attachment, basic

• Primary Device ID: B504OM222100230
• NIH Device Record Key: 46c461ea-fa5d-4b02-a644-9e7b50de1187
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: GEO
• Version Model Number: 22210023
• Company DUNS: 016889401
• Company Name: Provision
• Device Count: 1
• DM Exempt: true
• 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: true
• 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
HIBCC	B504OM222100230 [Primary]

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: 2024-09-24
• Device Publish Date: 2024-09-16

On-Brand Devices [GEO]

• B504OM273510080: 27351008
• B504OM270002300: 27000230
• B504OM262000450: 26200045
• B504OM221400450: 22140045
• B504OM221300300: 22130030
• B504OM220910080: 22091008
• B504OM210342000: 21034200
• B504OM200199200: 20019920
• B504OM221900000: 22190000
• B504OM221400550: 22140055
• B504OM210161000: 21016100
• B504OM270101500: 27010150
• B504OM210201000: 21020100
• B504OM214271000: 21427100
• B504OM210281500: 21028150
• B504OM200099200: 20009920
• B504OM240000010: 24000001
• B504OM223011120: 22301112
• B504OM223008100: 22300810
• B504OM214201000: 21420100
• B504OM230000360: 23000036
• B504OM221128500: 22112850
• B504OM212502300: 21250230
• B504OM201099300: 20109930
• B504OM222100230: 22210023