Biatain Silicone Non-Border

Basic Information

• Brand Name: Biatain Silicone Non-Border
• Primary DI: 05701780210676
• Version / Model: 39023
• Catalog Number: 39023
• Company Name: Coloplast A/S
• Labeler DUNS: 305524696
• Distribution Status: In Commercial Distribution
• Device Count in Pkg: 1
• Record Status: Published
• Publish Date: 2021-12-10
• Public Version: 1
• Public Version Date: 2021-12-22
• Public Version Status: New
• Public Device Record Key: ece0f3c7-7e0c-436f-af3c-3cf3cba67b16

Device Description

Biatain Silicone Non-Border . Non-Border foam dressing - with soft adhesion for general purposes. Klinikpackung. Dressing Length 12.5 cm, Dressing Length 5 in, Dressing Width 12.5 cm, Dressing Width 5 in.

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: Yes
• 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: Yes
• Has Donation ID: No

Sterilization

• Is Sterile: Yes
• Sterilization Prior Use: No

Product Codes

Code	Name	Medical Specialty	Regulation #	Device Class
NAD	Dressing, wound, occlusive	General, Plastic Surgery	878.4020	1

GMDN Terms

Code	Name	Definition	Implantable	Status
44970	Exudate-absorbent dressing, non-gel, non-antimicrobial	A wound covering intended to assist in wound healing by absorbing exudate in wounds (e.g., ulcers, burns, surgical wounds, lacerations, abrasions) and often by creating a moist wound-healing environment. It is not in the form of a gel and does not produce a water-absorbent gel upon contact with wound exudates, but may be designed to absorb and remove exudates (e.g., by capillary action); it does not contain an antimicrobial agent, but may include antioxidant properties. The device is available in a variety of forms (e.g., flat sheet/film-like, impregnated pouches, filled sachets, lyophilized matrix, ribbon, rope, foam, liquid, or powder). After application, this device cannot be reused.	No	Active

Identifiers

Type	ID	Issuing Agency	Package Type	Qty per Pkg	Pkg Status	Pkg Discontinue Date
Package	05701780174633	GS1	Shipper Box	12	In Commercial Distribution
Package	05701780174541	GS1	Retail Box	10	In Commercial Distribution
Primary	05701780210676	GS1

Customer Contacts

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

Device Sizes

Type	Value	Unit	Text
Width	5	Inch
Length	12.5	Centimeter
Width	12.5	Centimeter
Length	5	Inch

Storage Conditions

• Type: Special Storage Condition, Specify
• Special Conditions: This way up. Keep away from sunlight. Do not use if package is damaged and consult IFU.