BOSS Instruments

Basic Information

• Brand Name: BOSS Instruments
• Primary DI: 00888515051706
• Version / Model: 46-2290
• Catalog Number: 46-2290
• Company Name: BOSS INSTRUMENTS, LTD., INC.
• Labeler DUNS: 848522678
• Distribution Status: In Commercial Distribution
• Device Count in Pkg: 1
• Record Status: Published
• Publish Date: 2024-02-28
• Public Version: 1
• Public Version Date: 2024-03-07
• Public Version Status: New
• Public Device Record Key: e5e0d373-4d86-40c4-9d0c-a04ad3e19b4e

Device Description

Cohen Acorn Cannula, Intrauterine Probe, Spring-Mount Fcp

Device Characteristics

• Single Use: No
• Prescription Use (Rx): Yes
• 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
KOH	INSTRUMENT, MANUAL, GENERAL OBSTETRIC-GYNECOLOGIC	Obstetrics/Gynecology	884.4520	1

GMDN Terms

Code	Name	Definition	Implantable	Status
62163	Intrauterine cannula, reusable	A semi-rigid or rigid, plastic tube designed to be inserted into the uterus and connected to an aspirator/suction system pump to aspirate fluid/material from the uterus for treatment of incomplete abortion, first trimester abortion, and/or for menstrual regulation; it may also be intended for endometrial biopsy. This is a reusable device after appropriate sterilization/disinfection.	No	Active

Identifiers

Type	ID	Issuing Agency	Package Type	Qty per Pkg	Pkg Status	Pkg Discontinue Date
Primary	00888515051706	GS1

Customer Contacts

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