Lap-port closure device guides 5mm and 10/12 mm OS-LPCD - 5-10/12

GUDID B354OSLPCDG5101210

Lap-port closure device guides 5mm and 10/12 mm

ORANGE SURGICAL INSTRUMENTS, LLC

Endoscopic electrosurgical electrode, monopolar, single-use

• Primary Device ID: B354OSLPCDG5101210
• NIH Device Record Key: 09f2daf5-af44-44de-9b8a-e72021b42226
• Commercial Distribution Discontinuation: 2019-11-15
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Lap-port closure device guides 5mm and 10/12 mm
• Version Model Number: OS-LPCD-5-10/12
• Catalog Number: OS-LPCD - 5-10/12
• 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: true
• Lot Batch: true
• 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	B354OSLPCDG510120 [Primary]
HIBCC	B354OSLPCDG5101210 [Package]; Contains: B354OSLPCDG510120; Package: [10 Units]; Discontinued: 2019-11-15; Not in Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K101733

FDA Product Code

• GEI: Electrosurgical, Cutting & Coagulation & Accessories

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: 2019-11-15
• Device Publish Date: 2016-11-15

On-Brand Devices [Lap-port closure device guides 5mm and 10/12 mm]

• B354OSLPCDG5101210: Lap-port closure device guides 5mm and 10/12 mm
• B354OSLPCDG0: Lap-port closure device guides 5mm and 10/12 mm