CareFusion 2200

GUDID B504GSMO16500

Provision

Drilling power tool attachment, basic

• Primary Device ID: B504GSMO16500
• NIH Device Record Key: 1629d6d9-a8fa-4b3b-98f9-ebec5b5060a2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CareFusion 2200
• Version Model Number: MO1650
• 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	B504GSMO16500 [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

On-Brand Devices [CareFusion 2200]

• B504GSRH11450040: RH1145-004
• B504GSSU20140020: SU2014-002
• B504GSCH59020: CH5902
• B504GSOP23210: OP2321
• B504GSRH25620: RH2562
• B504GSSU1980A0: SU1980A
• B504GSRA47000070: RA4700-007
• B504GSNL14000: NL1400
• B504GSSU29050: SU2905
• B504GSSU27220: SU2722
• B50GSSA29050: SA2905
• B504GSRH47010090: RH4701-009
• B504GSSU160600: SU16060
• B504GSSU40550: SU4055
• B504OMCH56750: CH5675
• B504GSHS82320: HS8232
• B504GSSU29360: SU2936
• B504GSOP55250: OP5525
• B504GSMO16500: MO1650
• B504GSOA27200: OA2720