Tebbetts Type Septal Elevator, 4mm, Double Ended

GUDID B382SD93943010

Tebbetts Type Septal Elevator, 4mm, Double Ended

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

• Primary Device ID: B382SD93943010
• NIH Device Record Key: bcc30f50-e907-4717-b74c-ce13cce156a8
• Commercial Distribution Discontinuation: 2023-11-10
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Tebbetts Type Septal Elevator, 4mm, Double Ended
• Version Model Number: SD9394301
• 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	B382SD93943010 [Primary]

FDA Product Code

• GEI: Electrosurgical, Cutting & Coagulation & Accessories

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-11-20
• Device Publish Date: 2023-11-10

Devices Manufactured by ORANGE SURGICAL INSTRUMENTS, LLC

• B382SD93943010 - Tebbetts Type Septal Elevator, 4mm, Double Ended: 2023-11-20Tebbetts Type Septal Elevator, 4mm, Double Ended
• B382SD93943010 - Tebbetts Type Septal Elevator, 4mm, Double Ended: 2023-11-20 Tebbetts Type Septal Elevator, 4mm, Double Ended
• B3543690 - Maryland, Small Head Inner Shaft 10mm: 2023-08-15 Maryland, Small Head Inner Shaft 10mm
• B3543810 - Claw Forceps Inner Shaft 10mm: 2023-08-15 Claw Forceps Inner Shaft 10mm
• B3543820 - Claws Forceps Inner Shaft: 2023-08-15 Claws Forceps Inner Shaft
• B3543830 - Raptor/Wavy Inner Shaft: 2023-08-15 Raptor/Wavy Inner Shaft
• B3543970 - Allis Grasper Horizontal Teeth Inner Shaft: 2023-08-15 Allis Grasper Horizontal Teeth Inner Shaft
• B3543980 - Allis Grasper Vertical Teeth Inner Shaft: 2023-08-15 Allis Grasper Vertical Teeth Inner Shaft
• B3544440 - Handle for 10mm: 2023-08-15 Handle for 10mm