Surgical Direct

Basic Information

• Brand Name: Surgical Direct
• Primary DI: B382SD914715310
• Version / Model: SD91471531
• Catalog Number: SD91471531
• Company Name: Surgical Direct, Inc.
• Labeler DUNS: 124367223
• Distribution Status: In Commercial Distribution
• Device Count in Pkg: 1
• Record Status: Published
• Publish Date: 2023-02-21
• Public Version: 1
• Public Version Date: 2023-03-01
• Public Version Status: New
• Public Device Record Key: d80b6dad-3dfa-4cb2-8360-075a0bfe725e

Device Description

12 Inch Putti Bone Rasp, Round Blade, Double Ended

Device Characteristics

• Single Use: No
• Prescription Use (Rx): No
• Over the Counter (OTC): No
• Kit: No
• Combination Product: No
• HCT/P: No
• Contains NRL: No
• Not Made with NRL: No
• MRI Safety: Labeling does not contain MRI Safety Information
• Direct Marking Exempt: No
• PM Exempt: Yes
• Has Serial Number: No
• Has Lot/Batch Number: Yes
• Has Manufacturing Date: No
• Has Expiration Date: No
• Has Donation ID: No

Sterilization

• Is Sterile: No
• Sterilization Prior Use: Yes
• Sterilization Methods: Moist Heat or Steam Sterilization

Product Codes

Code	Name	Medical Specialty	Regulation #	Device Class
GEG	ELEVATOR, SURGICAL, GENERAL & PLASTIC SURGERY	General, Plastic Surgery	878.4800	1

GMDN Terms

Code	Name	Definition	Implantable	Status
11703	Callous file/rasp, reusable	A hand-held manual instrument with a surface(s) of coarse and/or fine grooves or teeth at the distal working end designed to be rubbed back and forth over the skin to remove callouses (i.e., hardened and thickened protrusions of skin commonly known as hard skin). This is a reusable device.	No	Active

Identifiers

Type	ID	Issuing Agency	Package Type	Qty per Pkg	Pkg Status	Pkg Discontinue Date
Primary	B382SD914715310	HIBCC

Customer Contacts

• Phone: [phone]
• Email: [email protected]