Arthrocare

GUDID 00810041063151

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 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 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: 00810041063151
• NIH Device Record Key: c8b9115e-bad7-4748-aa12-186aca895bd0
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Arthrocare
• Version Model Number: A2823-01
• Company DUNS: 016889401
• Company Name: Provision
• 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: 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
GS1	00810041063151 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K173741

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: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2020-04-30
• Device Publish Date: 2019-12-12

On-Brand Devices [Arthrocare ]

• B504EICA8872010: EICA8872-01
• B504EICA8870010: EICA8870-01
• B504EICA5872010: EICA5872-01
• B504CBEICA8872010: EICA8872-01
• B504CBEICA8870010: EICA8870-01
• B504CBEICA5872010: EICA5872-01
• B504ASC5500010: ASC5500-01
• B504ASC3730010: ASC3730-01
• B504AEASC5500010: ASC5500-01
• B504AEASC4250010: ASC4250-01
• B504AEASC3730010: ASC3730-01
• B504AEASC2530010: ASC2530-01
• B504AEAC4340010: AC4340-01
• B504AEAC4330010: AC4330-01
• B504AEAC4050010: AC4050-01
• B504AEAC3525010: AC3525-01
• B504AEAC2823010: AC2823-01
• B504AEAC2430010: AC2430-01
• B504AEAC1830010: AC1830-01
• B504AEAC1336010: AC1336-01
• B504AEAC1335010: AC1335-01
• B504AEA4330010: A4330-01
• B504AEA4300010: A4300-01
• B504AEA3625010: A3625-01
• B504AEA3525010: A3525-01
• B504AEA2823010: A2823-01
• B504AEA2723010: A2723-01
• B504AEA2630010: A2630-01
• B504AEA2530010: A2530-01
• B504AEA2430010: A2430-01
• B504AEA1830010: A1830-01
• B504AEA1730010: A1730-01
• B504AEA1720010: A1720-01
• B504AEA1336010: A1336-01
• B504AEA1335010: A1335-01
• B504AEA1325010: A1325-01
• B504AC4340010: AC4340-01
• B504AC4330010: AC4330-01
• B504AC4050010: AC4050-01
• B504AC3525010: AC3525-01
• B504AC2823010: AC2823-01
• B504AC2430010: AC2430-01
• B504AC1830010: AC1830-01
• B504AC1336010: AC1336-01
• B504A4330010: A4330-01
• B504A4300010: A4300-01
• B504A3625010: A3625-01
• B504A2823010: A2823-01
• B504A2630010: A2630-01
• B504A1720010: A1720-01