Smoke Pencil

GUDID B354OSSP0

Smoke Pencil

ORANGE SURGICAL INSTRUMENTS, LLC

Endoscopic electrosurgical handpiece/electrode, monopolar, reusable Endoscopic electrosurgical handpiece/electrode, monopolar, reusable Endoscopic electrosurgical handpiece/electrode, monopolar, reusable Endoscopic electrosurgical handpiece/electrode, monopolar, reusable Endoscopic electrosurgical handpiece/electrode, monopolar, reusable Endoscopic electrosurgical handpiece/electrode, monopolar, reusable Endoscopic electrosurgical handpiece/electrode, monopolar, reusable Endoscopic electrosurgical handpiece/electrode, monopolar, reusable Endoscopic electrosurgical handpiece/electrode, monopolar, reusable Endoscopic electrosurgical handpiece/electrode, monopolar, reusable Endoscopic electrosurgical handpiece/electrode, monopolar, reusable Endoscopic electrosurgical handpiece/electrode, monopolar, reusable Endoscopic electrosurgical handpiece/electrode, monopolar, reusable Endoscopic electrosurgical handpiece/electrode, monopolar, reusable Endoscopic electrosurgical handpiece/electrode, monopolar, reusable Endoscopic electrosurgical handpiece/electrode, monopolar, reusable Endoscopic electrosurgical handpiece/electrode, monopolar, reusable

• Primary Device ID: B354OSSP0
• NIH Device Record Key: 21e0f0c2-5295-42c0-8ff8-5006d2fee6b0
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Smoke Pencil
• Version Model Number: OSSP
• 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: false
• 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	B354OSSP0 [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

[B354OSSP0]

Peracetic Acid

[B354OSSP0]

Peracetic Acid

[B354OSSP0]

Peracetic Acid

[B354OSSP0]

Peracetic Acid

[B354OSSP0]

Peracetic Acid

[B354OSSP0]

Peracetic Acid

[B354OSSP0]

Peracetic Acid

[B354OSSP0]

Peracetic Acid

[B354OSSP0]

Peracetic Acid

[B354OSSP0]

Peracetic Acid

[B354OSSP0]

Peracetic Acid

[B354OSSP0]

Peracetic Acid

[B354OSSP0]

Peracetic Acid

[B354OSSP0]

Peracetic Acid

[B354OSSP0]

Peracetic Acid

[B354OSSP0]

Peracetic Acid

[B354OSSP0]

Peracetic Acid

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-02-01
• Device Publish Date: 2024-01-24

Devices Manufactured by ORANGE SURGICAL INSTRUMENTS, LLC

• B354OSLPCDG0 - Lap-port closure device guides 5mm and 10/12 mm: 2024-03-15 Lap-port closure device guides 5mm and 10/12 mm
• B354OS349440 - Needle Holder Straight 44cm: 2024-03-12 Needle Holder Straight 44cm
• B354CCBF14100 - Baton 10mm Foam: 2024-02-29 Baton 10mm Foam
• B354CCBF1450 - Baton 5mm Foam: 2024-02-29 Baton 5mm Foam
• B354CCLCS50 - Lens Cleaner 5mm - 10/12mm Batons with Foam Sleeve for 5mm Shaft: 2024-02-29 Lens Cleaner 5mm - 10/12mm Batons with Foam Sleeve for 5mm Shaft
• B354CCLCS80 - Lens Cleaner 5mm - 10/12mm Batons with Foam Sleeve for 8mm Shaft: 2024-02-29 Lens Cleaner 5mm - 10/12mm Batons with Foam Sleeve for 8mm Shaft
• B354CCS50 - Lens Cleaner Foam Sleeve for 5mm Shaft: 2024-02-29 Lens Cleaner Foam Sleeve for 5mm Shaft
• B354CCS5100 - 5mm x 10mm Foam Sleeves: 2024-02-29 5mm x 10mm Foam Sleeves