Richards

GUDID B504GS2308580

Provision

Drilling power tool attachment, basic

• Primary Device ID: B504GS2308580
• NIH Device Record Key: cd4e68bb-652d-4e10-afa0-a44ffd9c2c47
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Richards
• Version Model Number: 23-0858
• 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

Customer Support Contacts

• Phone: 541-508-7520
• Email: customersupport@provisiondrs.com
• Phone: 541-508-7520
• Email: customersupport@provisiondrs.com
• Phone: 541-508-7520
• Email: customersupport@provisiondrs.com
• Phone: 541-508-7520
• Email: customersupport@provisiondrs.com
• Phone: 541-508-7520
• Email: customersupport@provisiondrs.com
• Phone: 541-508-7520
• Email: customersupport@provisiondrs.com
• Phone: 541-508-7520
• Email: customersupport@provisiondrs.com
• Phone: 541-508-7520
• Email: customersupport@provisiondrs.com
• Phone: 541-508-7520
• Email: customersupport@provisiondrs.com
• Phone: 541-508-7520
• Email: customersupport@provisiondrs.com
• Phone: 541-508-7520
• Email: customersupport@provisiondrs.com
• Phone: 541-508-7520
• Email: customersupport@provisiondrs.com
• Phone: 541-508-7520
• Email: customersupport@provisiondrs.com
• Phone: 541-508-7520
• Email: customersupport@provisiondrs.com
• Phone: 541-508-7520
• Email: customersupport@provisiondrs.com
• Phone: 541-508-7520
• Email: customersupport@provisiondrs.com
• Phone: 541-508-7520
• Email: customersupport@provisiondrs.com

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	B504GS2308580 [Primary]

FDA Product Code

• KDC: Instrument, Surgical, Disposable

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: 2024-09-03
• Device Publish Date: 2024-08-26

Devices Manufactured by Provision

• B504OM13090119XG10 - Zimmer: 2025-12-03
• B504OM19100119XG10 - Zimmer: 2025-12-03
• B504OM20090119XC10 - Zimmer: 2025-12-03
• B504OM20100119XC10 - Zimmer: 2025-12-03
• B504OM20100119XCW0 - Zimmer: 2025-12-03
• B504OM21090119XGW0 - Zimmer: 2025-12-03
• B504OM17090127YGS0 - Zimmer: 2025-09-11
• B504OM0145080 - Smith and Nephew: 2025-06-27