Argent

GUDID 20612479212927

High Frequency Electrosurgical Generator/Desiccator

MCKESSON MEDICAL-SURGICAL INC.

Electrosurgical return electrode, reusable Electrosurgical return electrode, reusable Electrosurgical return electrode, reusable Electrosurgical return electrode, reusable Electrosurgical return electrode, reusable Electrosurgical return electrode, reusable Electrosurgical return electrode, reusable Electrosurgical return electrode, reusable Electrosurgical return electrode, reusable Electrosurgical return electrode, reusable Electrosurgical return electrode, reusable Electrosurgical return electrode, reusable Electrosurgical return electrode, reusable Electrosurgical return electrode, reusable Electrosurgical return electrode, reusable Electrosurgical return electrode, reusable Electrosurgical return electrode, reusable Electrosurgical return electrode, reusable Electrosurgical return electrode, reusable Electrosurgical return electrode, reusable Electrosurgical return electrode, reusable Electrosurgical return electrode, reusable Electrosurgical return electrode, reusable Electrosurgical return electrode, reusable Electrosurgical return electrode, reusable Electrosurgical return electrode, reusable Electrosurgical return electrode, reusable

• Primary Device ID: 20612479212927
• NIH Device Record Key: 482f863e-5d7d-4454-a140-e3c834a6cef1
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Argent
• Version Model Number: 22-A952
• Company DUNS: 023904428
• Company Name: MCKESSON MEDICAL-SURGICAL INC.
• 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: false
• Lot Batch: true
• Serial Number: true
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	10612479212913 [Direct Marking]
GS1	20612479212927 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K021817

FDA Product Code

• GEI: Electrosurgical, Cutting & Coagulation & Accessories

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2017-08-07

On-Brand Devices [Argent]

• 20612479212965: High Frequency Electrosurgical Desiccator
• 20612479212927: High Frequency Electrosurgical Generator/Desiccator
• 20612479210237: ELECTRODE, BALL EXT'D 5MM
• 20612479210220: ELECTRODE, BALL EXT 3MM
• 20612479210213: ELECTRODE LOOP 13X8MM
• 20612479210206: ELECTRODE, LOOP 20X20MM
• 20612479210190: ELECTRODE, LOOP 15MMX8MM
• 20612479210183: ELECTRODE LOOP 5MMX5MM
• 20612479209965: ELECTRODE, LOOP 20MMX8MM
• 20612479209958: ELECTRODE, LOOP 20MMX15MM
• 20612479209941: ELECTRODE, LOOP 20X10MM
• 20612479209934: ELECTRODE, LOOP 15MMX10MM
• 20612479209927: ELECTRODE, LOOP 10MMX10MM
• 20612479209910: ELECTRODE SQ 5MMX5MM
• 20612479209903: ELECTRODE SQ 10MMX8MM
• 20612479209897: ELECTRODE SQ 10MMX4MM
• 20612479209880: TIP, HYFRECATOR BLNT N/S
• 20612479209873: TIP, HYFRECATOR SHP N/S
• 20612479209866: TIP, HYFRECATOR BLNT
• 20612479209859: TIP, HYFRECATOR SHP STR
• 20612479209835: SHEATH, HANDPIECE STR 36"
• 20612479209828: SHEATH, HYFRECATOR N/S
• 10612479209067: CAUTERY, HI-TEMP VAS TIP
• 10612479209043: CAUTERY, HI-TEMP LOOP TIP
• 10612479209029: CAUTERY, HI-TEMP FINE