Mixter Inner Shaft C265

GUDID B354C2650

Mixter Inner Shaft

ORANGE SURGICAL INSTRUMENTS, LLC

Endoscopic electrosurgical electrode, monopolar, single-use Endoscopic electrosurgical electrode, monopolar, single-use Endoscopic electrosurgical electrode, monopolar, single-use Endoscopic electrosurgical electrode, monopolar, single-use Endoscopic electrosurgical electrode, monopolar, single-use Endoscopic electrosurgical electrode, monopolar, single-use Endoscopic electrosurgical electrode, monopolar, single-use Endoscopic electrosurgical electrode, monopolar, single-use Endoscopic electrosurgical electrode, monopolar, single-use Endoscopic electrosurgical electrode, monopolar, single-use Endoscopic electrosurgical electrode, monopolar, single-use Endoscopic electrosurgical electrode, monopolar, single-use Endoscopic electrosurgical electrode, monopolar, single-use Endoscopic electrosurgical electrode, monopolar, single-use Endoscopic electrosurgical electrode, monopolar, single-use Endoscopic electrosurgical electrode, monopolar, single-use Endoscopic electrosurgical electrode, monopolar, single-use Endoscopic electrosurgical electrode, monopolar, single-use Endoscopic electrosurgical electrode, monopolar, single-use Endoscopic electrosurgical electrode, monopolar, single-use Endoscopic electrosurgical electrode, monopolar, single-use Endoscopic electrosurgical electrode, monopolar, single-use Endoscopic electrosurgical electrode, monopolar, single-use Endoscopic electrosurgical electrode, monopolar, single-use Endoscopic electrosurgical electrode, monopolar, single-use Endoscopic electrosurgical electrode, monopolar, single-use Endoscopic electrosurgical electrode, monopolar, single-use

• Primary Device ID: B354C2650
• NIH Device Record Key: af49405a-a31d-4dab-aac5-5f9f95707a71
• Commercial Distribution Discontinuation: 2022-05-01
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Mixter Inner Shaft
• Version Model Number: C265
• Catalog Number: C265
• Company DUNS: 047063695
• Company Name: ORANGE SURGICAL INSTRUMENTS, LLC
• 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: false
• Serial Number: true
• Manufacturing Date: false
• 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
HIBCC	B354C2650 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K101733

FDA Product Code

• GEI: Electrosurgical, Cutting & Coagulation & Accessories

Sterilization

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

[B354C2650]

Peracetic Acid

[B354C2650]

Peracetic Acid

[B354C2650]

Peracetic Acid

[B354C2650]

Peracetic Acid

[B354C2650]

Peracetic Acid

[B354C2650]

Peracetic Acid

[B354C2650]

Peracetic Acid

[B354C2650]

Peracetic Acid

[B354C2650]

Peracetic Acid

[B354C2650]

Peracetic Acid

[B354C2650]

Peracetic Acid

[B354C2650]

Peracetic Acid

[B354C2650]

Peracetic Acid

[B354C2650]

Peracetic Acid

[B354C2650]

Peracetic Acid

[B354C2650]

Peracetic Acid

[B354C2650]

Peracetic Acid

[B354C2650]

Peracetic Acid

[B354C2650]

Peracetic Acid

[B354C2650]

Peracetic Acid

[B354C2650]

Peracetic Acid

[B354C2650]

Peracetic Acid

[B354C2650]

Peracetic Acid

[B354C2650]

Peracetic Acid

[B354C2650]

Peracetic Acid

[B354C2650]

Peracetic Acid

[B354C2650]

Peracetic Acid

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2019-05-09
• Device Publish Date: 2019-05-01

On-Brand Devices [Mixter Inner Shaft ]

• B354C2650: Mixter Inner Shaft
• B3542650: Mixter Inner Shaft