SenSura Click

Basic Information

• Brand Name: SenSura Click
• Primary DI: 05708932408691
• Version / Model: 10045
• Catalog Number: 10045
• Company Name: Coloplast A/S
• Labeler DUNS: 305524696
• Distribution Status: In Commercial Distribution
• Device Count in Pkg: 5
• Record Status: Published
• Publish Date: 2022-05-06
• Public Version: 1
• Public Version Date: 2022-05-16
• Public Version Status: New
• Public Device Record Key: 29d6453e-8114-4f36-b6ec-d15c5cf9033d

Device Description

SenSura Click / SenSura Click Click Xpro ostomy baseplate / Coloplast / Coloplast Click Xpro ostomy baseplate / SenSura Click SenSura Click Xpro ostomy baseplate / Coloplast SenSura Click Xpro ostomy baseplate / SenSura Product name: 2-piece Ostomy bag / SenSura Click Xpro ostomy baseplate. With belt ears. Not for individual sale. Registered trademark phrase for Mexico. Maxi. Coupling Size Diameter 70 mm, Coupling Size Diameter 2 3/4 in, Base Plate Precut Start Hole Size 10 mm, Base Plate Max Cut Size 65 mm, Baseplate Max Cut Size 2 9/16 in, Baseplate Precut Start Hole Size 3/8 in, Base Plate Type Flat.

Device Characteristics

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

Sterilization

• Is Sterile: No
• Sterilization Prior Use: No

Product Codes

Code	Name	Medical Specialty	Regulation #	Device Class
EXB	COLLECTOR, OSTOMY	Gastroenterology, Urology	876.5900	1

GMDN Terms

Code	Name	Definition	Implantable	Status
48159	Intestinal ostomy base plate, flat	A non-sterile device designed with a flat surface intended to be applied and adhered to peristomal skin (typically of a normal, well-formed stoma) to facilitate the correct positioning and anchorage of the flange of an intestinal ostomy bag (i.e., one-piece or exchangeable two-piece/multiple piece) and to protect the area from bodily waste contaminants. It is typically self-applied by the patient. This is a single-use device.	No	Active

Identifiers

Type	ID	Issuing Agency	Package Type	Qty per Pkg	Pkg Status	Pkg Discontinue Date
Package	05708932408707	GS1	Shipper Box	32	In Commercial Distribution
Primary	05708932408691	GS1
Unit of Use	05701780041706	GS1

Customer Contacts

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

Device Sizes

Type	Value	Unit	Text
Device Size Text, specify			Base Plate Max Cut Size - mm 65
Device Size Text, specify			Coupling Size Diameter - in 2 3/4
Device Size Text, specify			Base Plate Precut Start Hole Size - mm 10
Device Size Text, specify			Baseplate Precut Start Hole Size - in 3/8
Device Size Text, specify			Baseplate Max Cut Size - in 2 9/16
Lumen/Inner Diameter	70	Millimeter