MaxGuard, MaxPlus

Basic Information

• Brand Name: MaxGuard, MaxPlus
• Primary DI: 10885403236921
• Version / Model: MP9081-SF
• Catalog Number: MP9081-SF
• Company Name: BD Switzerland Sàrl
• Labeler DUNS: 482631558
• Distribution Status: Not in Commercial Distribution
• Device Count in Pkg: 1
• Record Status: Published
• Publish Date: 2016-09-22
• Public Version: 6
• Public Version Date: 2024-07-23
• Public Version Status: Update
• Public Device Record Key: 073b8335-cb87-40c0-a9b8-bbc40803fb74
• Distribution End Date: 2023-02-01

Device Description

8 IN KINK RESISTANT SET W/MAXPLUS

Device Characteristics

• Single Use: Yes
• 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: No
• Has Serial Number: No
• Has Lot/Batch Number: Yes
• Has Manufacturing Date: No
• Has Expiration Date: Yes
• Has Donation ID: No

Sterilization

• Is Sterile: Yes
• Sterilization Prior Use: No

Product Codes

Code	Name	Medical Specialty	Regulation #	Device Class
FPA	Set, administration, intravascular	General Hospital	880.5440	2

GMDN Terms

Code	Name	Definition	Implantable	Status
12170	Intravenous administration tubing extension set	A collection of tubing and connectors intended to establish an extension of tubing where the standard length of the tubing in an intravenous (IV) administration set is insufficient. This is a single-use device.	No	Active

Identifiers

Type	ID	Issuing Agency	Package Type	Qty per Pkg	Pkg Status	Pkg Discontinue Date
Package	20885403236928	GS1	Case	600	Not in Commercial Distribution	2023-02-01
Primary	10885403236921	GS1
Package	50885403236929	GS1	Shelfpack	50	Not in Commercial Distribution	2023-02-01

Customer Contacts

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

Storage Conditions

• Type: Special Storage Condition, Specify
• Special Conditions: Room Temperature