Guide Wire Dispenser

Basic Information

• Brand Name: Guide Wire Dispenser
• Primary DI: M73922311000
• Version / Model: 2231-1000
• Company Name: CAPTIVA SPINE, INC.
• Labeler DUNS: 836975784
• Distribution Status: In Commercial Distribution
• Device Count in Pkg: 1
• Record Status: Published
• Publish Date: 2022-07-23
• Public Version: 1
• Public Version Date: 2022-08-01
• Public Version Status: New
• Public Device Record Key: f2b698f6-4d14-4d86-bb81-a78dcead3ff8

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
LXH	Orthopedic Manual Surgical Instrument	Orthopedic	888.4540	1

GMDN Terms

Code	Name	Definition	Implantable	Status
61944	Guidewire holder	A sterile tubular device intended to be used for the storage and retrieval of one or more guidewires within the sterile field during a procedure. It is typically a long (approximately three metres) tube, that can be secured to surgical drapes, with a funnel-shaped proximal end and sometimes a sealed, vented distal end. This is a single-use device.	No	Active

Identifiers

Type	ID	Issuing Agency	Package Type	Qty per Pkg	Pkg Status	Pkg Discontinue Date
Primary	M73922311000	HIBCC

Customer Contacts

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