PRINCETON

Basic Information

• Brand Name: PRINCETON
• Primary DI: 00810158218246
• Version / Model: 21110-16
• Company Name: Princeton Medical Group, Inc.
• Labeler DUNS: 012857277
• Distribution Status: In Commercial Distribution
• Device Count in Pkg: 1
• Record Status: Published
• Publish Date: 2026-01-05
• Public Version: 1
• Public Version Date: 2026-01-13
• Public Version Status: New
• Public Device Record Key: ce77aff4-8912-4cb2-936e-0958ce26479a

Device Description

DIRECTOR GROOVED 6.25"

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
HXB	Probe	Orthopedic	888.4540	1

GMDN Terms

Code	Name	Definition	Implantable	Status
46486	Gastro-urological director	A slender, rod-like surgical instrument made of metal, typically with groove running along the centre of it distal shaft and/or continuing with an elongated malleable wire loop, that is used to guide other devices or instruments into a selected intracorporeal location during a gastroenterological/urological (GU) procedure. The distal shaft may be straight or curved and the proximal handle formed as a finger grip. This is a reusable device.	No	Active

Identifiers

Type	ID	Issuing Agency	Package Type	Qty per Pkg	Pkg Status	Pkg Discontinue Date
Primary	00810158218246	GS1