Medtronic

GUDID B504CB2332010

Provision

Endoscopic electrosurgical handpiece/electrode, bipolar, reprocessed Endoscopic electrosurgical handpiece/electrode, bipolar, reprocessed Endoscopic electrosurgical handpiece/electrode, bipolar, reprocessed Endoscopic electrosurgical handpiece/electrode, bipolar, reprocessed Endoscopic electrosurgical handpiece/electrode, bipolar, reprocessed Endoscopic electrosurgical handpiece/electrode, bipolar, reprocessed Endoscopic electrosurgical handpiece/electrode, bipolar, reprocessed

• Primary Device ID: B504CB2332010
• NIH Device Record Key: cb7ef043-6523-4d7a-a87d-e054c586b08d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Medtronic
• Version Model Number: 23-320-1
• Company DUNS: 016889401
• Company Name: Provision
• Device Count: 1
• DM Exempt: true
• 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: 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: 541-480-7953
• Email: customersupport@provisiondrs.com
• Phone: 541-480-7953
• Email: customersupport@provisiondrs.com
• Phone: 541-480-7953
• Email: customersupport@provisiondrs.com
• Phone: 541-480-7953
• Email: customersupport@provisiondrs.com
• Phone: 541-480-7953
• Email: customersupport@provisiondrs.com
• Phone: 541-480-7953
• Email: customersupport@provisiondrs.com
• Phone: 541-480-7953
• Email: customersupport@provisiondrs.com

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	B504CB2332010 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K172647

FDA Product Code

• NUJ: Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed

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: 2022-07-13
• Device Publish Date: 2022-07-05

On-Brand Devices [Medtronic]

• B504OM75BA50: 75BA50
• B504OM75BA300: 75BA30
• B504OM75BA400: 75BA40
• B504OM75BA20DCL0: 75BA20DCL
• B504OM75BA20DC0: 75BA20DC
• 08100410609199: 75BA50
• 08100410609182: 75BA40
• 08100410609175: 75BA30
• 08100410609168: 75BA20DCL
• 08100410609151: 75BA20DC
• 00810041069184: 75BA50
• 00810041069177: 75BA40
• 00810041069160: 75BA30
• 00810041069153: 75BA20DCL
• 00810041069146: 75BA20DC
• B504LGX30020000: X3-002-000
• B504LG3500710000: 350-071-000
• B504LG3500160000: 350-016-000
• B504LG3500140000: 350-014-000
• B504LG3500120000: 350-012-000
• 00810041639530: X3-002-000
• 00810041639523: 350-012-000
• 00810041639516: 350-014-000
• 00810041639509: 350-016-000
• 00810041639493: 350-071-000
• B504OM14MH30D0: 14MH30D
• B504OM14MH300: 14MH30
• 00810041639592: 14MH30D
• 00810041639585: 14MH30
• B504OMMC300: MC30
• B504OM15MH30D0: 15MH30D
• B504OM69751500: 6975150
• B504OM15MH17D0: 145M17D
• B504OMMR815MH220: MR8-15MH22
• B504OMMR814MH300: MR8-14MH30
• B504OM14BA600: 14BA60
• B504OM14BA500: 14BA50
• B504OMT12MH250: T12MH25
• B504OMMR815CY50DCD0: MR8-15CY50DCD
• B504OMT14MH30M0: T14MH30M
• B504OM14BA200: 14BA20
• B504CB2331310: 23-313-1
• B504OM8750880: 875-088
• B504GS858650: 85865
• B504OM15CY50DCD0: 15CY50DCD
• B504OMT14MH250: T14MH25
• B504OM86700010: 8670001
• B504CB2332010: 23-320-1
• B504OMMR87BA60C0: MR8-7BA60C
• B504OMMR87BA600: MR8-7BA60